rs730880758

Orientation

minus

Stabilized

minus

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

Make rs730880758(A;C)

Make rs730880758(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23424095

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880758
dbSNP (classic)	rs730880758
ClinGen	rs730880758
ebi	rs730880758
HLI	rs730880758
Exac	rs730880758
Gnomad	rs730880758
Varsome	rs730880758
LitVar	rs730880758
Map	rs730880758
PheGenI	rs730880758
Biobank	rs730880758
1000 genomes	rs730880758
hgdp	rs730880758
ensembl	rs730880758
geneview	rs730880758
scholar	rs730880758
google	rs730880758
pharmgkb	rs730880758
gwascentral	rs730880758
openSNP	rs730880758
23andMe	rs730880758
SNPshot	rs730880758
SNPdbe	rs730880758
MSV3d	rs730880758
GWAS Ctlg	rs730880758

Max Magnitude

0

ClinVar
Risk	rs730880758(C;C)
Alt	rs730880758(C;C)
Reference	Rs730880758(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23893304T>G
CLNSRC
CLNACC	RCV000158571.2,