rs397516275

Orientation

minus

Stabilized

minus

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

Make rs397516275(A;A)

Make rs397516275(A;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

23430591

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs397516275
dbSNP (classic)	rs397516275
ClinGen	rs397516275
ebi	rs397516275
HLI	rs397516275
Exac	rs397516275
Gnomad	rs397516275
Varsome	rs397516275
LitVar	rs397516275
Map	rs397516275
PheGenI	rs397516275
Biobank	rs397516275
1000 genomes	rs397516275
hgdp	rs397516275
ensembl	rs397516275
geneview	rs397516275
scholar	rs397516275
google	rs397516275
pharmgkb	rs397516275
gwascentral	rs397516275
openSNP	rs397516275
23andMe	rs397516275
SNPshot	rs397516275
SNPdbe	rs397516275
MSV3d	rs397516275
GWAS Ctlg	rs397516275

Max Magnitude

0

ClinVar
Risk	rs397516275(A;A) rs397516275(C;C) rs397516275(G;G)
Alt	rs397516275(A;A) rs397516275(C;C) rs397516275(G;G)
Reference	Rs397516275(T;T)
Significance	Probable-Pathogenic
Disease	not specified Cardiovascular phenotype
Variation	info
Gene	MYH7
CLNDBN	not specified Cardiovascular phenotype
Reversed	1
HGVS	NC_000014.8:g.23899800A>G; NC_000014.8:g.23899800A>T
CLNSRC	ClinVar
CLNACC	RCV000036013.3, RCV000251862.1, RCV000036012.4,