rs730880772

Orientation

minus

Stabilized

minus

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

Make rs730880772(C;C)

Make rs730880772(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23421025

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880772
dbSNP (classic)	rs730880772
ClinGen	rs730880772
ebi	rs730880772
HLI	rs730880772
Exac	rs730880772
Gnomad	rs730880772
Varsome	rs730880772
LitVar	rs730880772
Map	rs730880772
PheGenI	rs730880772
Biobank	rs730880772
1000 genomes	rs730880772
hgdp	rs730880772
ensembl	rs730880772
geneview	rs730880772
scholar	rs730880772
google	rs730880772
pharmgkb	rs730880772
gwascentral	rs730880772
openSNP	rs730880772
23andMe	rs730880772
SNPshot	rs730880772
SNPdbe	rs730880772
MSV3d	rs730880772
GWAS Ctlg	rs730880772

Max Magnitude

0

ClinVar
Risk	rs730880772(C;C)
Alt	rs730880772(C;C)
Reference	Rs730880772(T;T)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	MYH7
CLNDBN	not specified
Reversed	1
HGVS	NC_000014.8:g.23890234A>G
CLNSRC
CLNACC	RCV000158599.2,