rs730880751

Orientation

minus

Stabilized

minus

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

Make rs730880751(C;C)

Make rs730880751(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23424816

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880751
dbSNP (classic)	rs730880751
ClinGen	rs730880751
ebi	rs730880751
HLI	rs730880751
Exac	rs730880751
Gnomad	rs730880751
Varsome	rs730880751
LitVar	rs730880751
Map	rs730880751
PheGenI	rs730880751
Biobank	rs730880751
1000 genomes	rs730880751
hgdp	rs730880751
ensembl	rs730880751
geneview	rs730880751
scholar	rs730880751
google	rs730880751
pharmgkb	rs730880751
gwascentral	rs730880751
openSNP	rs730880751
23andMe	rs730880751
SNPshot	rs730880751
SNPdbe	rs730880751
MSV3d	rs730880751
GWAS Ctlg	rs730880751

Max Magnitude

0

ClinVar
Risk	rs730880751(C;C)
Alt	rs730880751(C;C)
Reference	Rs730880751(G;G)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	MYH7
CLNDBN	not specified
Reversed	1
HGVS	NC_000014.8:g.23894025C>G
CLNSRC
CLNACC	RCV000158556.2,