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rs281860494

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860494(A;A)
Make rs281860494(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271212
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860494
ebirs281860494
HLIrs281860494
Exacrs281860494
Varsomers281860494
Maprs281860494
PheGenIrs281860494
hapmaprs281860494
1000 genomesrs281860494
hgdprs281860494
ensemblrs281860494
gopubmedrs281860494
geneviewrs281860494
scholarrs281860494
googlers281860494
pharmgkbrs281860494
gwascentralrs281860494
openSNPrs281860494
23andMers281860494
23andMe allrs281860494
SNP Nexus

SNPshotrs281860494
SNPdbers281860494
MSV3drs281860494
GWAS Ctlgrs281860494
Max Magnitude0
ClinVar
Risk rs281860494(A,C;A,C)
Alt rs281860494(A,C;A,C)
Reference rs281860494(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238989C>G; NC_000006.11:g.31238989C>T
CLNSRC
CLNACC