rs730880891

Orientation

minus

Stabilized

minus

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

Make rs730880891(-;-)

Make rs730880891(-;TGC)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23417664

Gene	MHRT, MIR208B, MYH7

is a	snp
is	mentioned by
dbSNP	rs730880891
dbSNP (classic)	rs730880891
ClinGen	rs730880891
ebi	rs730880891
HLI	rs730880891
Exac	rs730880891
Gnomad	rs730880891
Varsome	rs730880891
LitVar	rs730880891
Map	rs730880891
PheGenI	rs730880891
Biobank	rs730880891
1000 genomes	rs730880891
hgdp	rs730880891
ensembl	rs730880891
geneview	rs730880891
scholar	rs730880891
google	rs730880891
pharmgkb	rs730880891
gwascentral	rs730880891
openSNP	rs730880891
23andMe	rs730880891
SNPshot	rs730880891
SNPdbe	rs730880891
MSV3d	rs730880891
GWAS Ctlg	rs730880891

Max Magnitude

0

ClinVar
Risk	rs730880891(-;-)
Alt	rs730880891(-;-)
Reference	Rs730880891(TGC;TGC)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	MYH7 MHRT MIR208B
CLNDBN	not specified
Reversed	1
HGVS	NC_000014.8:g.23886873_23886875delGCA
CLNSRC
CLNACC	RCV000158833.2,