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rs863224052

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224052(A;A)
Make rs863224052(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position43894567
GeneLRPPRC
is asnp
is mentioned by
dbSNPrs863224052
ebirs863224052
HLIrs863224052
Exacrs863224052
Varsomers863224052
Maprs863224052
PheGenIrs863224052
hapmaprs863224052
1000 genomesrs863224052
hgdprs863224052
ensemblrs863224052
gopubmedrs863224052
geneviewrs863224052
scholarrs863224052
googlers863224052
pharmgkbrs863224052
gwascentralrs863224052
openSNPrs863224052
23andMers863224052
23andMe allrs863224052
SNP Nexus

SNPshotrs863224052
SNPdbers863224052
MSV3drs863224052
GWAS Ctlgrs863224052
Max Magnitude0
ClinVar
Risk rs863224052(A;A)
Alt rs863224052(A;A)
Reference rs863224052(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene LRPPRC
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.44121706G>T
CLNSRC
CLNACC RCV000200227.1,