rs267606881

Orientation

plus

Stabilized

plus

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

Make rs267606881(A;A)

Make rs267606881(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

MT

Position

8529

Gene

ATP6

is a	snp
is	mentioned by
dbSNP	rs267606881
dbSNP (classic)	rs267606881
ClinGen	rs267606881
ebi	rs267606881
HLI	rs267606881
Exac	rs267606881
Gnomad	rs267606881
Varsome	rs267606881
LitVar	rs267606881
Map	rs267606881
PheGenI	rs267606881
Biobank	rs267606881
1000 genomes	rs267606881
hgdp	rs267606881
ensembl	rs267606881
geneview	rs267606881
scholar	rs267606881
google	rs267606881
pharmgkb	rs267606881
gwascentral	rs267606881
openSNP	rs267606881
23andMe	rs267606881
SNPshot	rs267606881
SNPdbe	rs267606881
MSV3d	rs267606881
GWAS Ctlg	rs267606881

Max Magnitude

0

ClinVar
Risk	rs267606881(A;A)
Alt	rs267606881(A;A)
Reference	Rs267606881(G;G)
Significance	Pathogenic
Disease	Cardiomyopathy
Variation	info
Gene	ATP6
CLNDBN	Cardiomyopathy, apical hypertrophic, and neuropathy
Reversed	0
HGVS	NC_012920.1:m.8529G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000010271.3,