rs150415679

Orientation

plus

Stabilized

plus

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

Make rs150415679(C;T)

Make rs150415679(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23398866

Gene

MYH6

is a	snp
is	mentioned by
dbSNP	rs150415679
dbSNP (classic)	rs150415679
ClinGen	rs150415679
ebi	rs150415679
HLI	rs150415679
Exac	rs150415679
Gnomad	rs150415679
Varsome	rs150415679
LitVar	rs150415679
Map	rs150415679
PheGenI	rs150415679
Biobank	rs150415679
1000 genomes	rs150415679
hgdp	rs150415679
ensembl	rs150415679
geneview	rs150415679
scholar	rs150415679
google	rs150415679
pharmgkb	rs150415679
gwascentral	rs150415679
openSNP	rs150415679
23andMe	rs150415679
SNPshot	rs150415679
SNPdbe	rs150415679
MSV3d	rs150415679
GWAS Ctlg	rs150415679

Max Magnitude

0

ClinVar
Risk	rs150415679(T;T)
Alt	rs150415679(T;T)
Reference	Rs150415679(C;C)
Significance	Probable-non-pathogenic
Disease	Cardiomyopathy not specified Cardiovascular phenotype Dilated Cardiomyopathy Atrial septal defect Hypertrophic cardiomyopathy
Variation	info
Gene	MYH6
CLNDBN	Cardiomyopathy not specified Cardiovascular phenotype Dilated Cardiomyopathy, Dominant Atrial septal defect Hypertrophic cardiomyopathy
Reversed	0
HGVS	NC_000014.8:g.23868075C>T
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030305.1, RCV000037446.2, RCV000250070.1, RCV000304935.1, RCV000343459.1, RCV000405421.1,