rs397516259

Orientation

minus

Stabilized

minus

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

Make rs397516259(A;A)

Make rs397516259(A;C)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23431790

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs397516259
dbSNP (classic)	rs397516259
ClinGen	rs397516259
ebi	rs397516259
HLI	rs397516259
Exac	rs397516259
Gnomad	rs397516259
Varsome	rs397516259
LitVar	rs397516259
Map	rs397516259
PheGenI	rs397516259
Biobank	rs397516259
1000 genomes	rs397516259
hgdp	rs397516259
ensembl	rs397516259
geneview	rs397516259
scholar	rs397516259
google	rs397516259
pharmgkb	rs397516259
gwascentral	rs397516259
openSNP	rs397516259
23andMe	rs397516259
SNPshot	rs397516259
SNPdbe	rs397516259
MSV3d	rs397516259
GWAS Ctlg	rs397516259

Max Magnitude

0

ClinVar
Risk	rs397516259(A;A) rs397516259(T;T)
Alt	rs397516259(A;A) rs397516259(T;T)
Reference	Rs397516259(C;C)
Significance	Pathogenic
Disease	not provided not specified
Variation	info
Gene	MYH7
CLNDBN	not provided not specified
Reversed	1
HGVS	NC_000014.8:g.23900999G>A; NC_000014.8:g.23900999G>T
CLNSRC
CLNACC	RCV000158748.1, RCV000035989.3,