rs730880796

Orientation

minus

Stabilized

minus

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

Make rs730880796(C;T)

Make rs730880796(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23417618

Gene	MHRT, MIR208B, MYH7

is a	snp
is	mentioned by
dbSNP	rs730880796
dbSNP (classic)	rs730880796
ClinGen	rs730880796
ebi	rs730880796
HLI	rs730880796
Exac	rs730880796
Gnomad	rs730880796
Varsome	rs730880796
LitVar	rs730880796
Map	rs730880796
PheGenI	rs730880796
Biobank	rs730880796
1000 genomes	rs730880796
hgdp	rs730880796
ensembl	rs730880796
geneview	rs730880796
scholar	rs730880796
google	rs730880796
pharmgkb	rs730880796
gwascentral	rs730880796
openSNP	rs730880796
23andMe	rs730880796
SNPshot	rs730880796
SNPdbe	rs730880796
MSV3d	rs730880796
GWAS Ctlg	rs730880796

Max Magnitude

0

ClinVar
Risk	rs730880796(A;A) rs730880796(T;T)
Alt	rs730880796(A;A) rs730880796(T;T)
Reference	Rs730880796(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7 MHRT MIR208B
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23886827G>A
CLNSRC
CLNACC	RCV000158645.2,