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rs281860522

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860522(A;A)
Make rs281860522(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271139
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860522
ebirs281860522
HLIrs281860522
Exacrs281860522
Varsomers281860522
Maprs281860522
PheGenIrs281860522
hapmaprs281860522
1000 genomesrs281860522
hgdprs281860522
ensemblrs281860522
gopubmedrs281860522
geneviewrs281860522
scholarrs281860522
googlers281860522
pharmgkbrs281860522
gwascentralrs281860522
openSNPrs281860522
23andMers281860522
23andMe allrs281860522
SNP Nexus

SNPshotrs281860522
SNPdbers281860522
MSV3drs281860522
GWAS Ctlgrs281860522
Max Magnitude0
ClinVar
Risk rs281860522(A,C;A,C)
Alt rs281860522(A,C;A,C)
Reference rs281860522(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238916C>G; NC_000006.11:g.31238916C>T
CLNSRC
CLNACC