rs730880792

Orientation

minus

Stabilized

minus

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

Make rs730880792(A;A)

Make rs730880792(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

23418220

Gene	MIR208B, MYH7

is a	snp
is	mentioned by
dbSNP	rs730880792
dbSNP (classic)	rs730880792
ClinGen	rs730880792
ebi	rs730880792
HLI	rs730880792
Exac	rs730880792
Gnomad	rs730880792
Varsome	rs730880792
LitVar	rs730880792
Map	rs730880792
PheGenI	rs730880792
Biobank	rs730880792
1000 genomes	rs730880792
hgdp	rs730880792
ensembl	rs730880792
geneview	rs730880792
scholar	rs730880792
google	rs730880792
pharmgkb	rs730880792
gwascentral	rs730880792
openSNP	rs730880792
23andMe	rs730880792
SNPshot	rs730880792
SNPdbe	rs730880792
MSV3d	rs730880792
GWAS Ctlg	rs730880792

Max Magnitude

0

ClinVar
Risk	rs730880792(A;A) rs730880792(C;C)
Alt	rs730880792(A;A) rs730880792(C;C)
Reference	Rs730880792(G;G)
Significance	Probable-Pathogenic
Disease	not specified Hypertrophic cardiomyopathy
Variation	info
Gene	MYH7 MIR208B
CLNDBN	not specified Hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000014.8:g.23887429C>T
CLNSRC
CLNACC	RCV000158638.2, RCV000457747.1,