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

rs281860580

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs281860580(A;A)
Make rs281860580(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270083
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860580
ebirs281860580
HLIrs281860580
Exacrs281860580
Varsomers281860580
Maprs281860580
PheGenIrs281860580
hapmaprs281860580
1000 genomesrs281860580
hgdprs281860580
ensemblrs281860580
gopubmedrs281860580
geneviewrs281860580
scholarrs281860580
googlers281860580
pharmgkbrs281860580
gwascentralrs281860580
openSNPrs281860580
23andMers281860580
23andMe allrs281860580
SNP Nexus

SNPshotrs281860580
SNPdbers281860580
MSV3drs281860580
GWAS Ctlgrs281860580
Max Magnitude0
ClinVar
Risk rs281860580(A;A)
Alt rs281860580(A;A)
Reference rs281860580(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237860G>T
CLNSRC
CLNACC