rs201327273

Orientation

plus

Stabilized

plus

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

Make rs201327273(A;T)

Make rs201327273(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23403422

Gene

MYH6

is a	snp
is	mentioned by
dbSNP	rs201327273
dbSNP (classic)	rs201327273
ClinGen	rs201327273
ebi	rs201327273
HLI	rs201327273
Exac	rs201327273
Gnomad	rs201327273
Varsome	rs201327273
LitVar	rs201327273
Map	rs201327273
PheGenI	rs201327273
Biobank	rs201327273
1000 genomes	rs201327273
hgdp	rs201327273
ensembl	rs201327273
geneview	rs201327273
scholar	rs201327273
google	rs201327273
pharmgkb	rs201327273
gwascentral	rs201327273
openSNP	rs201327273
23andMe	rs201327273
SNPshot	rs201327273
SNPdbe	rs201327273
MSV3d	rs201327273
GWAS Ctlg	rs201327273

Max Magnitude

0

ClinVar
Risk	rs201327273(T;T)
Alt	rs201327273(T;T)
Reference	Rs201327273(A;A)
Significance	Probable-Pathogenic
Disease	not specified Primary dilated cardiomyopathy Familial hypertrophic cardiomyopathy 14
Variation	info
Gene	MYH6
CLNDBN	not specified Primary dilated cardiomyopathy Familial hypertrophic cardiomyopathy 14
Reversed	0
HGVS	NC_000014.8:g.23872631A>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000037541.2, RCV000171837.2, RCV000470174.1,