rs863225108

Merged into

rs727504288

Orientation

minus

Stabilized

minus

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

Make rs863225108(-;-)

Make rs863225108(-;AAG)

Make rs863225108(AAG;AAG)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

47337560

Gene

MYBPC3

is a	snp
is	mentioned by
dbSNP	rs863225108
dbSNP (classic)	rs863225108
ClinGen	rs863225108
ebi	rs863225108
HLI	rs863225108
Exac	rs863225108
Gnomad	rs863225108
Varsome	rs863225108
LitVar	rs863225108
Map	rs863225108
PheGenI	rs863225108
Biobank	rs863225108
1000 genomes	rs863225108
hgdp	rs863225108
ensembl	rs863225108
geneview	rs863225108
scholar	rs863225108
google	rs863225108
pharmgkb	rs863225108
gwascentral	rs863225108
openSNP	rs863225108
23andMe	rs863225108
SNPshot	rs863225108
SNPdbe	rs863225108
MSV3d	rs863225108
GWAS Ctlg	rs863225108

Status

Merged into rs727504288

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs863225108(AGA;AGA)
Significance	Other
Disease	not specified Primary familial hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 4 Hypertrophic cardiomyopathy
Variation	info
Gene	MYBPC3
CLNDBN	not specified Primary familial hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 4 Hypertrophic cardiomyopathy
Reversed	1
HGVS	NC_000011.9:g.47359101_47359103delTCT
CLNSRC	Children's Hospital of Eastern Ontario
CLNACC	RCV000154301.2, RCV000157327.3, RCV000168801.2, RCV000196806.2,