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Genome Assembly
Position and Type
Variant ID
dbSNP rsid
Reference Location
Variation Type
All
SNP
InDel
Consequence Type
HIGH
MODERATE
LOW
MODIFIER
Annotation Gene Information
Gene ID
Upstream
Downstream
Gene Symbol
Gramene ID
UniprotKB
Biotype
mRNA
rRNA
miRNA
Ontology Term
Ontology Key Words
Minor Allele Frequency
MAF
>=
<=
=
(0-0.5)
ClinVar Traits
Effect
affects
benign
likely benign
likely pathogenic
pathogenic
uncertain significance
association
drug response
not reported for simple variant
protective
risk factor
other
Initial
A(617)
B(256)
C(790)
D(383)
E(256)
F(264)
G(261)
H(1215)
I(179)
J(50)
K(49)
L(264)
M(659)
N(201)
O(147)
P(540)
Q(2)
R(186)
S(485)
T(189)
U(37)
V(65)
W(60)
X(25)
Y(4)
Z(9)
Digit(29)
Other(3)
OMIM Traits
Initial
A(550)
B(245)
C(777)
D(300)
E(255)
F(200)
G(278)
H(1302)
I(136)
J(40)
K(36)
L(256)
M(708)
N(211)
O(142)
P(472)
R(189)
S(442)
T(206)
<
U(29)
V(66)
W(63)
X(14)
Y(2)
Z(2)
Digit(36)
GWAS-Catalog Traits
Ontology
immune system disease(EFO_0000540)
body weights and measures(EFO_0004324)
cancer(EFO_0000311)
cardiovascular disease(EFO_0000319)
cardiovascular measurement(EFO_0004298)
digestive system disease(EFO_0000405)
hematological measurement(EFO_0004503)
inflammatory biomarker measurement(EFO_0004872)
lipid or lipoprotein measurement(EFO_0005105)
liver enzyme measurement(EFO_0004582)
metabolic disease(EFO_0000589)
nervous system disease(EFO_0000618)
response to drug(GO_0042493)
other
Genotype to Phenotype
growth
drought tolerance
metabolite
agronomic traits
resistance
flowering time
forage quality
yield
Pfam
Pfam Accession
Pfam Name
Protein Id
Setting Properties
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Search Results: 40350378
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VarID
Position
Alleles
MAF
Consequence Type|Effect
Gene
dbSNP
gmx60169698
Chr01:8
T/G
T:0.5000
intergenic_variant|MODIFIER;
gmx22974108
Chr01:27
A/G
G:0.0017
intergenic_variant|MODIFIER;
gmx22974109
Chr01:35
G/C
C:0.0193
intergenic_variant|MODIFIER;
gmx3
Chr01:36
G/A
A:0.1021
intergenic_variant|MODIFIER;
gmx60169699
Chr01:37
T/G
T:0.5000
intergenic_variant|MODIFIER;
gmx75886138
Chr01:39
T/G
-:-
intergenic_variant|MODIFIER;
rs5994754263
gmx60169700
Chr01:42
C/G
G:0.5000
intergenic_variant|MODIFIER;
gmx61061947
Chr01:44
G/A
A:0.5000
intergenic_variant|MODIFIER;
gmx60169701
Chr01:49
G/C
C:0.5000
intergenic_variant|MODIFIER;
gmx60169702
Chr01:63
T/G,A
G:0.5000
intergenic_variant|MODIFIER;
rs743537926
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