rs863225096

Orientation

minus

Stabilized

minus

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

Make rs863225096(C;C)

Make rs863225096(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

23419926

Gene	MIR208B, MYH7

is a	snp
is	mentioned by
dbSNP	rs863225096
dbSNP (classic)	rs863225096
ClinGen	rs863225096
ebi	rs863225096
HLI	rs863225096
Exac	rs863225096
Gnomad	rs863225096
Varsome	rs863225096
LitVar	rs863225096
Map	rs863225096
PheGenI	rs863225096
Biobank	rs863225096
1000 genomes	rs863225096
hgdp	rs863225096
ensembl	rs863225096
geneview	rs863225096
scholar	rs863225096
google	rs863225096
pharmgkb	rs863225096
gwascentral	rs863225096
openSNP	rs863225096
23andMe	rs863225096
SNPshot	rs863225096
SNPdbe	rs863225096
MSV3d	rs863225096
GWAS Ctlg	rs863225096

Max Magnitude

0

ClinVar
Risk	rs863225096(C;C)
Alt	rs863225096(C;C)
Reference	Rs863225096(G;G)
Significance	Probable-Pathogenic
Disease	Familial hypertrophic cardiomyopathy 1
Variation	info
Gene	MYH7 MIR208B
CLNDBN	Familial hypertrophic cardiomyopathy 1
Reversed	1
HGVS	NC_000014.8:g.23889135C>G
CLNSRC
CLNACC	RCV000201442.1,