rs779869631

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs779869631(C;C)

Make rs779869631(C;G)

Reference

GRCh38.p7 38.3/149

Chromosome

7

Position

138762983

Gene

ATP6V0A4

is a	snp
is	mentioned by
dbSNP	rs779869631
dbSNP (classic)	rs779869631
ClinGen	rs779869631
ebi	rs779869631
HLI	rs779869631
Exac	rs779869631
Gnomad	rs779869631
Varsome	rs779869631
LitVar	rs779869631
Map	rs779869631
PheGenI	rs779869631
Biobank	rs779869631
1000 genomes	rs779869631
hgdp	rs779869631
ensembl	rs779869631
geneview	rs779869631
scholar	rs779869631
google	rs779869631
pharmgkb	rs779869631
gwascentral	rs779869631
openSNP	rs779869631
23andMe	rs779869631
SNPshot	rs779869631
SNPdbe	rs779869631
MSV3d	rs779869631
GWAS Ctlg	rs779869631

Max Magnitude

0

ClinVar
Risk	rs779869631(A;A) rs779869631(C;C)
Alt	rs779869631(A;A) rs779869631(C;C)
Reference	Rs779869631(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ATP6V0A4
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.138447728G>A
CLNSRC
CLNACC	RCV000287838.1,