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

rs281860408

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860408(A;A)
Make rs281860408(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271651
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860408
ebirs281860408
HLIrs281860408
Exacrs281860408
Varsomers281860408
Maprs281860408
PheGenIrs281860408
hapmaprs281860408
1000 genomesrs281860408
hgdprs281860408
ensemblrs281860408
gopubmedrs281860408
geneviewrs281860408
scholarrs281860408
googlers281860408
pharmgkbrs281860408
gwascentralrs281860408
openSNPrs281860408
23andMers281860408
23andMe allrs281860408
SNP Nexus

SNPshotrs281860408
SNPdbers281860408
MSV3drs281860408
GWAS Ctlgrs281860408
Max Magnitude0
ClinVar
Risk rs281860408(A;A)
Alt rs281860408(A;A)
Reference rs281860408(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239428A>T
CLNSRC
CLNACC