Have questions? Visit https://www.reddit.com/r/SNPedia

rs863225121

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225121(G;T)
Make rs863225121(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position74094449
GeneVCL
is asnp
is mentioned by
dbSNPrs863225121
ebirs863225121
HLIrs863225121
Exacrs863225121
Varsomers863225121
Maprs863225121
PheGenIrs863225121
hapmaprs863225121
1000 genomesrs863225121
hgdprs863225121
ensemblrs863225121
gopubmedrs863225121
geneviewrs863225121
scholarrs863225121
googlers863225121
pharmgkbrs863225121
gwascentralrs863225121
openSNPrs863225121
23andMers863225121
23andMe allrs863225121
SNP Nexus

SNPshotrs863225121
SNPdbers863225121
MSV3drs863225121
GWAS Ctlgrs863225121
Max Magnitude0
ClinVar
Risk rs863225121(T;T)
Alt rs863225121(T;T)
Reference rs863225121(G;G)
Significance Probable-Pathogenic
Disease Familial hypertrophic cardiomyopathy 15
Variation info
Gene VCL
CLNDBN Familial hypertrophic cardiomyopathy 15
Reversed 0
HGVS NC_000010.10:g.75854207G>T
CLNSRC
CLNACC RCV000201438.1,