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rs281860527

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860527(A;A)
Make rs281860527(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271128
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860527
ebirs281860527
HLIrs281860527
Exacrs281860527
Varsomers281860527
Maprs281860527
PheGenIrs281860527
hapmaprs281860527
1000 genomesrs281860527
hgdprs281860527
ensemblrs281860527
gopubmedrs281860527
geneviewrs281860527
scholarrs281860527
googlers281860527
pharmgkbrs281860527
gwascentralrs281860527
openSNPrs281860527
23andMers281860527
23andMe allrs281860527
SNP Nexus

SNPshotrs281860527
SNPdbers281860527
MSV3drs281860527
GWAS Ctlgrs281860527
Max Magnitude0
ClinVar
Risk rs281860527(A,G;A,G)
Alt rs281860527(A,G;A,G)
Reference rs281860527(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238905G>C; NC_000006.11:g.31238905G>T
CLNSRC
CLNACC