rs397516162

Orientation

minus

Stabilized

minus

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

Make rs397516162(C;G)

Make rs397516162(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23424146

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs397516162
dbSNP (classic)	rs397516162
ClinGen	rs397516162
ebi	rs397516162
HLI	rs397516162
Exac	rs397516162
Gnomad	rs397516162
Varsome	rs397516162
LitVar	rs397516162
Map	rs397516162
PheGenI	rs397516162
Biobank	rs397516162
1000 genomes	rs397516162
hgdp	rs397516162
ensembl	rs397516162
geneview	rs397516162
scholar	rs397516162
google	rs397516162
pharmgkb	rs397516162
gwascentral	rs397516162
openSNP	rs397516162
23andMe	rs397516162
SNPshot	rs397516162
SNPdbe	rs397516162
MSV3d	rs397516162
GWAS Ctlg	rs397516162

Max Magnitude

0

ClinVar
Risk	rs397516162(A;A) rs397516162(G;G)
Alt	rs397516162(A;A) rs397516162(G;G)
Reference	Rs397516162(C;C)
Significance	Probable-Pathogenic
Disease	not specified Hypertrophic cardiomyopathy
Variation	info
Gene	MYH7
CLNDBN	not specified Hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000014.8:g.23893355G>C; NC_000014.8:g.23893355G>T
CLNSRC	Children's Hospital of Eastern Ontario
CLNACC	RCV000035813.3, RCV000168877.3, RCV000457072.1,