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rs281860431

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860431(A;A)
Make rs281860431(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271607
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860431
ebirs281860431
HLIrs281860431
Exacrs281860431
Varsomers281860431
Maprs281860431
PheGenIrs281860431
hapmaprs281860431
1000 genomesrs281860431
hgdprs281860431
ensemblrs281860431
gopubmedrs281860431
geneviewrs281860431
scholarrs281860431
googlers281860431
pharmgkbrs281860431
gwascentralrs281860431
openSNPrs281860431
23andMers281860431
23andMe allrs281860431
SNP Nexus

SNPshotrs281860431
SNPdbers281860431
MSV3drs281860431
GWAS Ctlgrs281860431
Max Magnitude0
ClinVar
Risk rs281860431(A;A)
Alt rs281860431(A;A)
Reference rs281860431(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239384C>T
CLNSRC
CLNACC