Have questions? Visit https://www.reddit.com/r/SNPedia

rs281860561

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860561(A;A)
Make rs281860561(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270369
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860561
ebirs281860561
HLIrs281860561
Exacrs281860561
Varsomers281860561
Maprs281860561
PheGenIrs281860561
hapmaprs281860561
1000 genomesrs281860561
hgdprs281860561
ensemblrs281860561
gopubmedrs281860561
geneviewrs281860561
scholarrs281860561
googlers281860561
pharmgkbrs281860561
gwascentralrs281860561
openSNPrs281860561
23andMers281860561
23andMe allrs281860561
SNP Nexus

SNPshotrs281860561
SNPdbers281860561
MSV3drs281860561
GWAS Ctlgrs281860561
Max Magnitude0
ClinVar
Risk rs281860561(A;A)
Alt rs281860561(A;A)
Reference rs281860561(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238146C>T
CLNSRC
CLNACC