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rs863224058

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224058(C;T)
Make rs863224058(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position43899235
GeneLRPPRC
is asnp
is mentioned by
dbSNPrs863224058
ebirs863224058
HLIrs863224058
Exacrs863224058
Varsomers863224058
Maprs863224058
PheGenIrs863224058
hapmaprs863224058
1000 genomesrs863224058
hgdprs863224058
ensemblrs863224058
gopubmedrs863224058
geneviewrs863224058
scholarrs863224058
googlers863224058
pharmgkbrs863224058
gwascentralrs863224058
openSNPrs863224058
23andMers863224058
23andMe allrs863224058
SNP Nexus

SNPshotrs863224058
SNPdbers863224058
MSV3drs863224058
GWAS Ctlgrs863224058
Max Magnitude0
ClinVar
Risk rs863224058(T;T)
Alt rs863224058(T;T)
Reference rs863224058(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LRPPRC
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.44126374G>A
CLNSRC
CLNACC RCV000199926.2,