rs863225269

Orientation

minus

Stabilized

minus

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

Make rs863225269(-;C)

Make rs863225269(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

23392970

Gene

MYH6

is a	snp
is	mentioned by
dbSNP	rs863225269
dbSNP (classic)	rs863225269
ClinGen	rs863225269
ebi	rs863225269
HLI	rs863225269
Exac	rs863225269
Gnomad	rs863225269
Varsome	rs863225269
LitVar	rs863225269
Map	rs863225269
PheGenI	rs863225269
Biobank	rs863225269
1000 genomes	rs863225269
hgdp	rs863225269
ensembl	rs863225269
geneview	rs863225269
scholar	rs863225269
google	rs863225269
pharmgkb	rs863225269
gwascentral	rs863225269
openSNP	rs863225269
23andMe	rs863225269
SNPshot	rs863225269
SNPdbe	rs863225269
MSV3d	rs863225269
GWAS Ctlg	rs863225269

Max Magnitude

0

ClinVar
Risk	rs863225269(C;C)
Alt	rs863225269(C;C)
Reference	Rs863225269(-;-)
Significance	Pathogenic
Disease	Familial hypertrophic cardiomyopathy 1
Variation	info
Gene	MYH6
CLNDBN	Familial hypertrophic cardiomyopathy 1
Reversed	1
HGVS	NC_000014.8:g.23862180dupG
CLNSRC
CLNACC	RCV000201905.1,