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rs281860571

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860571(A;A)
Make rs281860571(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270240
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860571
ebirs281860571
HLIrs281860571
Exacrs281860571
Varsomers281860571
Maprs281860571
PheGenIrs281860571
hapmaprs281860571
1000 genomesrs281860571
hgdprs281860571
ensemblrs281860571
gopubmedrs281860571
geneviewrs281860571
scholarrs281860571
googlers281860571
pharmgkbrs281860571
gwascentralrs281860571
openSNPrs281860571
23andMers281860571
23andMe allrs281860571
SNP Nexus

SNPshotrs281860571
SNPdbers281860571
MSV3drs281860571
GWAS Ctlgrs281860571
Max Magnitude0
ClinVar
Risk rs281860571(A;A)
Alt rs281860571(A;A)
Reference rs281860571(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238017C>T
CLNSRC
CLNACC