rs267606905

Orientation

minus

Stabilized

minus

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

Make rs267606905(A;A)

Make rs267606905(A;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23387914

Gene

MYH6

is a	snp
is	mentioned by
dbSNP	rs267606905
dbSNP (classic)	rs267606905
ClinGen	rs267606905
ebi	rs267606905
HLI	rs267606905
Exac	rs267606905
Gnomad	rs267606905
Varsome	rs267606905
LitVar	rs267606905
Map	rs267606905
PheGenI	rs267606905
Biobank	rs267606905
1000 genomes	rs267606905
hgdp	rs267606905
ensembl	rs267606905
geneview	rs267606905
scholar	rs267606905
google	rs267606905
pharmgkb	rs267606905
gwascentral	rs267606905
openSNP	rs267606905
23andMe	rs267606905
SNPshot	rs267606905
SNPdbe	rs267606905
MSV3d	rs267606905
GWAS Ctlg	rs267606905

Max Magnitude

0

ClinVar
Risk	rs267606905(A;A)
Alt	rs267606905(A;A)
Reference	Rs267606905(G;G)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 1EE
Variation	info
Gene	MYH6
CLNDBN	Dilated cardiomyopathy 1EE
Reversed	1
HGVS	NC_000014.8:g.23857123C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015215.25,