rs730880731

Orientation

minus

Stabilized

minus

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

Make rs730880731(C;C)

Make rs730880731(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23426063

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880731
dbSNP (classic)	rs730880731
ClinGen	rs730880731
ebi	rs730880731
HLI	rs730880731
Exac	rs730880731
Gnomad	rs730880731
Varsome	rs730880731
LitVar	rs730880731
Map	rs730880731
PheGenI	rs730880731
Biobank	rs730880731
1000 genomes	rs730880731
hgdp	rs730880731
ensembl	rs730880731
geneview	rs730880731
scholar	rs730880731
google	rs730880731
pharmgkb	rs730880731
gwascentral	rs730880731
openSNP	rs730880731
23andMe	rs730880731
SNPshot	rs730880731
SNPdbe	rs730880731
MSV3d	rs730880731
GWAS Ctlg	rs730880731

Max Magnitude

0

ClinVar
Risk	rs730880731(C;C)
Alt	rs730880731(C;C)
Reference	Rs730880731(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23895272A>G
CLNSRC
CLNACC	RCV000158505.1,