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

rs281860487

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860487(A;A)
Make rs281860487(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271235
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860487
ebirs281860487
HLIrs281860487
Exacrs281860487
Varsomers281860487
Maprs281860487
PheGenIrs281860487
hapmaprs281860487
1000 genomesrs281860487
hgdprs281860487
ensemblrs281860487
gopubmedrs281860487
geneviewrs281860487
scholarrs281860487
googlers281860487
pharmgkbrs281860487
gwascentralrs281860487
openSNPrs281860487
23andMers281860487
23andMe allrs281860487
SNP Nexus

SNPshotrs281860487
SNPdbers281860487
MSV3drs281860487
GWAS Ctlgrs281860487
Max Magnitude0
ClinVar
Risk rs281860487(A,C,T;A,C,T)
Alt rs281860487(A,C,T;A,C,T)
Reference rs281860487(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239012C>A; NC_000006.11:g.31239012C>G; NC_000006.11:g.31239012C>T
CLNSRC
CLNACC