rs763982675
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs763982675(A;A) |
Make rs763982675(A;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 7 |
Position | 138747514 |
Gene | ATP6V0A4 |
is a | snp |
is | mentioned by |
dbSNP | rs763982675 |
dbSNP (classic) | rs763982675 |
ClinGen | rs763982675 |
ebi | rs763982675 |
HLI | rs763982675 |
Exac | rs763982675 |
Gnomad | rs763982675 |
Varsome | rs763982675 |
LitVar | rs763982675 |
Map | rs763982675 |
PheGenI | rs763982675 |
Biobank | rs763982675 |
1000 genomes | rs763982675 |
hgdp | rs763982675 |
ensembl | rs763982675 |
geneview | rs763982675 |
scholar | rs763982675 |
rs763982675 | |
pharmgkb | rs763982675 |
gwascentral | rs763982675 |
openSNP | rs763982675 |
23andMe | rs763982675 |
SNPshot | rs763982675 |
SNPdbe | rs763982675 |
MSV3d | rs763982675 |
GWAS Ctlg | rs763982675 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs763982675(A;A) |
Alt | rs763982675(A;A) |
Reference | Rs763982675(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | ATP6V0A4 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000007.13:g.138432259C>A |
CLNSRC | |
CLNACC | RCV000442300.1, |