rs267606904

Orientation

minus

Stabilized

minus

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

Make rs267606904(C;C)

Make rs267606904(C;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23392968

Gene

MYH6

is a	snp
is	mentioned by
dbSNP	rs267606904
dbSNP (classic)	rs267606904
ClinGen	rs267606904
ebi	rs267606904
HLI	rs267606904
Exac	rs267606904
Gnomad	rs267606904
Varsome	rs267606904
LitVar	rs267606904
Map	rs267606904
PheGenI	rs267606904
Biobank	rs267606904
1000 genomes	rs267606904
hgdp	rs267606904
ensembl	rs267606904
geneview	rs267606904
scholar	rs267606904
google	rs267606904
pharmgkb	rs267606904
gwascentral	rs267606904
openSNP	rs267606904
23andMe	rs267606904
SNPshot	rs267606904
SNPdbe	rs267606904
MSV3d	rs267606904
GWAS Ctlg	rs267606904

Max Magnitude

0

ClinVar
Risk	rs267606904(C;C)
Alt	rs267606904(C;C)
Reference	Rs267606904(G;G)
Significance	Other
Disease	Familial hypertrophic cardiomyopathy 14 not specified Primary familial hypertrophic cardiomyopathy Dilated cardiomyopathy Hemiplegia Migraine
Variation	info
Gene	MYH6
CLNDBN	Familial hypertrophic cardiomyopathy 14 not specified Primary familial hypertrophic cardiomyopathy Dilated cardiomyopathy Hemiplegia Migraine
Reversed	1
HGVS	NC_000014.8:g.23862177C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015212.26, RCV000037469.3, RCV000171836.1, RCV000414926.1,