rs730880788

Orientation

minus

Stabilized

minus

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

Make rs730880788(C;C)

Make rs730880788(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23418309

Gene	MIR208B, MYH7

is a	snp
is	mentioned by
dbSNP	rs730880788
dbSNP (classic)	rs730880788
ClinGen	rs730880788
ebi	rs730880788
HLI	rs730880788
Exac	rs730880788
Gnomad	rs730880788
Varsome	rs730880788
LitVar	rs730880788
Map	rs730880788
PheGenI	rs730880788
Biobank	rs730880788
1000 genomes	rs730880788
hgdp	rs730880788
ensembl	rs730880788
geneview	rs730880788
scholar	rs730880788
google	rs730880788
pharmgkb	rs730880788
gwascentral	rs730880788
openSNP	rs730880788
23andMe	rs730880788
SNPshot	rs730880788
SNPdbe	rs730880788
MSV3d	rs730880788
GWAS Ctlg	rs730880788

Max Magnitude

0

ClinVar
Risk	rs730880788(C;C)
Alt	rs730880788(C;C)
Reference	Rs730880788(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MYH7 MIR208B
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.23887518A>G
CLNSRC
CLNACC	RCV000158631.1,