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rs863224053

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224053(C;C)
Make rs863224053(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position43975089
GeneLRPPRC
is asnp
is mentioned by
dbSNPrs863224053
ebirs863224053
HLIrs863224053
Exacrs863224053
Varsomers863224053
Maprs863224053
PheGenIrs863224053
hapmaprs863224053
1000 genomesrs863224053
hgdprs863224053
ensemblrs863224053
gopubmedrs863224053
geneviewrs863224053
scholarrs863224053
googlers863224053
pharmgkbrs863224053
gwascentralrs863224053
openSNPrs863224053
23andMers863224053
23andMe allrs863224053
SNP Nexus

SNPshotrs863224053
SNPdbers863224053
MSV3drs863224053
GWAS Ctlgrs863224053
Max Magnitude0
ClinVar
Risk rs863224053(C;C)
Alt rs863224053(C;C)
Reference rs863224053(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene LRPPRC
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.44202228A>G
CLNSRC
CLNACC RCV000197365.1,