rs397516101

Orientation

minus

Stabilized

minus

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

Make rs397516101(A;A)

Make rs397516101(A;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23429004

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs397516101
dbSNP (classic)	rs397516101
ClinGen	rs397516101
ebi	rs397516101
HLI	rs397516101
Exac	rs397516101
Gnomad	rs397516101
Varsome	rs397516101
LitVar	rs397516101
Map	rs397516101
PheGenI	rs397516101
Biobank	rs397516101
1000 genomes	rs397516101
hgdp	rs397516101
ensembl	rs397516101
geneview	rs397516101
scholar	rs397516101
google	rs397516101
pharmgkb	rs397516101
gwascentral	rs397516101
openSNP	rs397516101
23andMe	rs397516101
SNPshot	rs397516101
SNPdbe	rs397516101
MSV3d	rs397516101
GWAS Ctlg	rs397516101

Max Magnitude

0

ClinVar
Risk	rs397516101(A;A) rs397516101(T;T)
Alt	rs397516101(A;A) rs397516101(T;T)
Reference	Rs397516101(G;G)
Significance	Other
Disease	not specified Primary familial hypertrophic cardiomyopathy not provided Hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 1
Variation	info
Gene	MYH7
CLNDBN	not specified Primary familial hypertrophic cardiomyopathy not provided Hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 1
Reversed	1
HGVS	NC_000014.8:g.23898213C>A; NC_000014.8:g.23898213C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000223878.1, RCV000035718.2, RCV000158800.1, RCV000195545.2, RCV000201462.1,