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rs281860448

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860448(A;A)
Make rs281860448(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271326
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860448
ebirs281860448
HLIrs281860448
Exacrs281860448
Varsomers281860448
Maprs281860448
PheGenIrs281860448
hapmaprs281860448
1000 genomesrs281860448
hgdprs281860448
ensemblrs281860448
gopubmedrs281860448
geneviewrs281860448
scholarrs281860448
googlers281860448
pharmgkbrs281860448
gwascentralrs281860448
openSNPrs281860448
23andMers281860448
23andMe allrs281860448
SNP Nexus

SNPshotrs281860448
SNPdbers281860448
MSV3drs281860448
GWAS Ctlgrs281860448
Max Magnitude0
ClinVar
Risk rs281860448(A;A)
Alt rs281860448(A;A)
Reference rs281860448(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239103C>T
CLNSRC
CLNACC