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rs281860491

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860491(C;G)
Make rs281860491(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271224
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860491
ebirs281860491
HLIrs281860491
Exacrs281860491
Varsomers281860491
Maprs281860491
PheGenIrs281860491
hapmaprs281860491
1000 genomesrs281860491
hgdprs281860491
ensemblrs281860491
gopubmedrs281860491
geneviewrs281860491
scholarrs281860491
googlers281860491
pharmgkbrs281860491
gwascentralrs281860491
openSNPrs281860491
23andMers281860491
23andMe allrs281860491
SNP Nexus

SNPshotrs281860491
SNPdbers281860491
MSV3drs281860491
GWAS Ctlgrs281860491
Max Magnitude0
ClinVar
Risk rs281860491(G,T;G,T)
Alt rs281860491(G,T;G,T)
Reference rs281860491(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239001G>A; NC_000006.11:g.31239001G>C
CLNSRC
CLNACC