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rs281860562

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860562(A;A)
Make rs281860562(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270367
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860562
ebirs281860562
HLIrs281860562
Exacrs281860562
Varsomers281860562
Maprs281860562
PheGenIrs281860562
hapmaprs281860562
1000 genomesrs281860562
hgdprs281860562
ensemblrs281860562
gopubmedrs281860562
geneviewrs281860562
scholarrs281860562
googlers281860562
pharmgkbrs281860562
gwascentralrs281860562
openSNPrs281860562
23andMers281860562
23andMe allrs281860562
SNP Nexus

SNPshotrs281860562
SNPdbers281860562
MSV3drs281860562
GWAS Ctlgrs281860562
Max Magnitude0
ClinVar
Risk rs281860562(A;A)
Alt rs281860562(A;A)
Reference rs281860562(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238144C>T
CLNSRC
CLNACC