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rs863224124

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224124(A;A)
Make rs863224124(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position31673487
GeneNUBPL
is asnp
is mentioned by
dbSNPrs863224124
ebirs863224124
HLIrs863224124
Exacrs863224124
Varsomers863224124
Maprs863224124
PheGenIrs863224124
hapmaprs863224124
1000 genomesrs863224124
hgdprs863224124
ensemblrs863224124
gopubmedrs863224124
geneviewrs863224124
scholarrs863224124
googlers863224124
pharmgkbrs863224124
gwascentralrs863224124
openSNPrs863224124
23andMers863224124
23andMe allrs863224124
SNP Nexus

SNPshotrs863224124
SNPdbers863224124
MSV3drs863224124
GWAS Ctlgrs863224124
Max Magnitude0
ClinVar
Risk rs863224124(A;A)
Alt rs863224124(A;A)
Reference rs863224124(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NUBPL
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.32142693G>A
CLNSRC
CLNACC RCV000198994.2,