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rs281860417

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860417(A;A)
Make rs281860417(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271633
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860417
ebirs281860417
HLIrs281860417
Exacrs281860417
Varsomers281860417
Maprs281860417
PheGenIrs281860417
hapmaprs281860417
1000 genomesrs281860417
hgdprs281860417
ensemblrs281860417
gopubmedrs281860417
geneviewrs281860417
scholarrs281860417
googlers281860417
pharmgkbrs281860417
gwascentralrs281860417
openSNPrs281860417
23andMers281860417
23andMe allrs281860417
SNP Nexus

SNPshotrs281860417
SNPdbers281860417
MSV3drs281860417
GWAS Ctlgrs281860417
Max Magnitude0
ClinVar
Risk rs281860417(A;A)
Alt rs281860417(A;A)
Reference rs281860417(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239410C>T
CLNSRC
CLNACC