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rs281860461

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860461(A;A)
Make rs281860461(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271297
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860461
ebirs281860461
HLIrs281860461
Exacrs281860461
Varsomers281860461
Maprs281860461
PheGenIrs281860461
hapmaprs281860461
1000 genomesrs281860461
hgdprs281860461
ensemblrs281860461
gopubmedrs281860461
geneviewrs281860461
scholarrs281860461
googlers281860461
pharmgkbrs281860461
gwascentralrs281860461
openSNPrs281860461
23andMers281860461
23andMe allrs281860461
SNP Nexus

SNPshotrs281860461
SNPdbers281860461
MSV3drs281860461
GWAS Ctlgrs281860461
Max Magnitude0
ClinVar
Risk rs281860461(A,T;A,T)
Alt rs281860461(A,T;A,T)
Reference rs281860461(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239074C>A; NC_000006.11:g.31239074C>T
CLNSRC
CLNACC