rs267606906

Orientation

minus

Stabilized

minus

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

Make rs267606906(C;T)

Make rs267606906(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23394264

Gene

MYH6

is a	snp
is	mentioned by
dbSNP	rs267606906
dbSNP (classic)	rs267606906
ClinGen	rs267606906
ebi	rs267606906
HLI	rs267606906
Exac	rs267606906
Gnomad	rs267606906
Varsome	rs267606906
LitVar	rs267606906
Map	rs267606906
PheGenI	rs267606906
Biobank	rs267606906
1000 genomes	rs267606906
hgdp	rs267606906
ensembl	rs267606906
geneview	rs267606906
scholar	rs267606906
google	rs267606906
pharmgkb	rs267606906
gwascentral	rs267606906
openSNP	rs267606906
23andMe	rs267606906
SNPshot	rs267606906
SNPdbe	rs267606906
MSV3d	rs267606906
GWAS Ctlg	rs267606906

Max Magnitude

0

ClinVar
Risk	rs267606906(T;T)
Alt	rs267606906(T;T)
Reference	Rs267606906(C;C)
Significance	Pathogenic
Disease	Dilated cardiomyopathy 1EE
Variation	info
Gene	MYH6
CLNDBN	Dilated cardiomyopathy 1EE
Reversed	1
HGVS	NC_000014.8:g.23863473G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015213.25,