rs730880857

Orientation

minus

Stabilized

minus

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

Make rs730880857(C;C)

Make rs730880857(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23430925

Gene

MYH7

is a	snp
is	mentioned by
dbSNP	rs730880857
dbSNP (classic)	rs730880857
ClinGen	rs730880857
ebi	rs730880857
HLI	rs730880857
Exac	rs730880857
Gnomad	rs730880857
Varsome	rs730880857
LitVar	rs730880857
Map	rs730880857
PheGenI	rs730880857
Biobank	rs730880857
1000 genomes	rs730880857
hgdp	rs730880857
ensembl	rs730880857
geneview	rs730880857
scholar	rs730880857
google	rs730880857
pharmgkb	rs730880857
gwascentral	rs730880857
openSNP	rs730880857
23andMe	rs730880857
SNPshot	rs730880857
SNPdbe	rs730880857
MSV3d	rs730880857
GWAS Ctlg	rs730880857

Max Magnitude

0

ClinVar
Risk	rs730880857(C;C)
Alt	rs730880857(C;C)
Reference	Rs730880857(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23900134A>G
CLNSRC
CLNACC	RCV000158770.2,