rs267606907

Orientation

minus

Stabilized

minus

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

Make rs267606907(A;A)

Make rs267606907(A;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23396329

Gene

MYH6

is a	snp
is	mentioned by
dbSNP	rs267606907
dbSNP (classic)	rs267606907
ClinGen	rs267606907
ebi	rs267606907
HLI	rs267606907
Exac	rs267606907
Gnomad	rs267606907
Varsome	rs267606907
LitVar	rs267606907
Map	rs267606907
PheGenI	rs267606907
Biobank	rs267606907
1000 genomes	rs267606907
hgdp	rs267606907
ensembl	rs267606907
geneview	rs267606907
scholar	rs267606907
google	rs267606907
pharmgkb	rs267606907
gwascentral	rs267606907
openSNP	rs267606907
23andMe	rs267606907
SNPshot	rs267606907
SNPdbe	rs267606907
MSV3d	rs267606907
GWAS Ctlg	rs267606907

Max Magnitude

0

ClinVar
Risk	rs267606907(A;A)
Alt	rs267606907(A;A)
Reference	Rs267606907(G;G)
Significance	Pathogenic
Disease	Familial hypertrophic cardiomyopathy 14
Variation	info
Gene	MYH6
CLNDBN	Familial hypertrophic cardiomyopathy 14
Reversed	1
HGVS	NC_000014.8:g.23865538C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015210.21,