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rs863224057

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224057(G;G)
Make rs863224057(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position43943768
GeneLRPPRC
is asnp
is mentioned by
dbSNPrs863224057
ebirs863224057
HLIrs863224057
Exacrs863224057
Varsomers863224057
Maprs863224057
PheGenIrs863224057
hapmaprs863224057
1000 genomesrs863224057
hgdprs863224057
ensemblrs863224057
gopubmedrs863224057
geneviewrs863224057
scholarrs863224057
googlers863224057
pharmgkbrs863224057
gwascentralrs863224057
openSNPrs863224057
23andMers863224057
23andMe allrs863224057
SNP Nexus

SNPshotrs863224057
SNPdbers863224057
MSV3drs863224057
GWAS Ctlgrs863224057
Max Magnitude0
ClinVar
Risk rs863224057(G;G)
Alt rs863224057(G;G)
Reference rs863224057(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LRPPRC
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.44170907A>C
CLNSRC
CLNACC RCV000198012.2,