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rs281860496

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860496(A;A)
Make rs281860496(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271203
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860496
ebirs281860496
HLIrs281860496
Exacrs281860496
Varsomers281860496
Maprs281860496
PheGenIrs281860496
hapmaprs281860496
1000 genomesrs281860496
hgdprs281860496
ensemblrs281860496
gopubmedrs281860496
geneviewrs281860496
scholarrs281860496
googlers281860496
pharmgkbrs281860496
gwascentralrs281860496
openSNPrs281860496
23andMers281860496
23andMe allrs281860496
SNP Nexus

SNPshotrs281860496
SNPdbers281860496
MSV3drs281860496
GWAS Ctlgrs281860496
Max Magnitude0
ClinVar
Risk rs281860496(A;A)
Alt rs281860496(A;A)
Reference rs281860496(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238980C>T
CLNSRC
CLNACC