rs730880799

Orientation

minus

Stabilized

minus

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

Make rs730880799(A;T)

Make rs730880799(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23417576

Gene	MHRT, MIR208B, MYH7

is a	snp
is	mentioned by
dbSNP	rs730880799
dbSNP (classic)	rs730880799
ClinGen	rs730880799
ebi	rs730880799
HLI	rs730880799
Exac	rs730880799
Gnomad	rs730880799
Varsome	rs730880799
LitVar	rs730880799
Map	rs730880799
PheGenI	rs730880799
Biobank	rs730880799
1000 genomes	rs730880799
hgdp	rs730880799
ensembl	rs730880799
geneview	rs730880799
scholar	rs730880799
google	rs730880799
pharmgkb	rs730880799
gwascentral	rs730880799
openSNP	rs730880799
23andMe	rs730880799
SNPshot	rs730880799
SNPdbe	rs730880799
MSV3d	rs730880799
GWAS Ctlg	rs730880799

Max Magnitude

0

ClinVar
Risk	rs730880799(T;T)
Alt	rs730880799(T;T)
Reference	Rs730880799(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7 MIR208B MHRT
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23886785T>A
CLNSRC
CLNACC	RCV000158651.2,