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rs281860472

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860472(A;A)
Make rs281860472(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271263
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860472
ebirs281860472
HLIrs281860472
Exacrs281860472
Varsomers281860472
Maprs281860472
PheGenIrs281860472
hapmaprs281860472
1000 genomesrs281860472
hgdprs281860472
ensemblrs281860472
gopubmedrs281860472
geneviewrs281860472
scholarrs281860472
googlers281860472
pharmgkbrs281860472
gwascentralrs281860472
openSNPrs281860472
23andMers281860472
23andMe allrs281860472
SNP Nexus

SNPshotrs281860472
SNPdbers281860472
MSV3drs281860472
GWAS Ctlgrs281860472
Max Magnitude0
ClinVar
Risk rs281860472(A,G,T;A,G,T)
Alt rs281860472(A,G,T;A,G,T)
Reference rs281860472(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239040G>A; NC_000006.11:g.31239040G>C; NC_000006.11:g.31239040G>T
CLNSRC
CLNACC