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rs763982675

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs763982675(A;A)
Make rs763982675(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position138747514
GeneATP6V0A4
is asnp
is mentioned by
dbSNPrs763982675
dbSNP (classic)rs763982675
ClinGenrs763982675
ebirs763982675
HLIrs763982675
Exacrs763982675
Gnomadrs763982675
Varsomers763982675
LitVarrs763982675
Maprs763982675
PheGenIrs763982675
Biobankrs763982675
1000 genomesrs763982675
hgdprs763982675
ensemblrs763982675
geneviewrs763982675
scholarrs763982675
googlers763982675
pharmgkbrs763982675
gwascentralrs763982675
openSNPrs763982675
23andMers763982675
23andMe allrs763982675
SNPshotrs763982675
SNPdbers763982675
MSV3drs763982675
GWAS Ctlgrs763982675
Max Magnitude0
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,