Have questions? Visit https://www.reddit.com/r/SNPedia

rs863224123

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224123(A;A)
Make rs863224123(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position31673483
GeneNUBPL
is asnp
is mentioned by
dbSNPrs863224123
ebirs863224123
HLIrs863224123
Exacrs863224123
Varsomers863224123
Maprs863224123
PheGenIrs863224123
hapmaprs863224123
1000 genomesrs863224123
hgdprs863224123
ensemblrs863224123
gopubmedrs863224123
geneviewrs863224123
scholarrs863224123
googlers863224123
pharmgkbrs863224123
gwascentralrs863224123
openSNPrs863224123
23andMers863224123
23andMe allrs863224123
SNP Nexus

SNPshotrs863224123
SNPdbers863224123
MSV3drs863224123
GWAS Ctlgrs863224123
Max Magnitude0
ClinVar
Risk rs863224123(A;A)
Alt rs863224123(A;A)
Reference rs863224123(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NUBPL
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.32142689G>A
CLNSRC
CLNACC RCV000197858.1,