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rs281860541

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs281860541(A;C)
Make rs281860541(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271102
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860541
ebirs281860541
HLIrs281860541
Exacrs281860541
Varsomers281860541
Maprs281860541
PheGenIrs281860541
hapmaprs281860541
1000 genomesrs281860541
hgdprs281860541
ensemblrs281860541
gopubmedrs281860541
geneviewrs281860541
scholarrs281860541
googlers281860541
pharmgkbrs281860541
gwascentralrs281860541
openSNPrs281860541
23andMers281860541
23andMe allrs281860541
SNP Nexus

SNPshotrs281860541
SNPdbers281860541
MSV3drs281860541
GWAS Ctlgrs281860541
Max Magnitude0
ClinVar
Risk rs281860541(C;C)
Alt rs281860541(C;C)
Reference rs281860541(A;A)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238879T>G
CLNSRC
CLNACC