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rs281860516

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860516(A;A)
Make rs281860516(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271155
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860516
ebirs281860516
HLIrs281860516
Exacrs281860516
Varsomers281860516
Maprs281860516
PheGenIrs281860516
hapmaprs281860516
1000 genomesrs281860516
hgdprs281860516
ensemblrs281860516
gopubmedrs281860516
geneviewrs281860516
scholarrs281860516
googlers281860516
pharmgkbrs281860516
gwascentralrs281860516
openSNPrs281860516
23andMers281860516
23andMe allrs281860516
SNP Nexus

SNPshotrs281860516
SNPdbers281860516
MSV3drs281860516
GWAS Ctlgrs281860516
Max Magnitude0
ClinVar
Risk rs281860516(A;A)
Alt rs281860516(A;A)
Reference rs281860516(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238932C>T
CLNSRC
CLNACC