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rs281860544

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860544(A;A)
Make rs281860544(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271092
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860544
ebirs281860544
HLIrs281860544
Exacrs281860544
Varsomers281860544
Maprs281860544
PheGenIrs281860544
hapmaprs281860544
1000 genomesrs281860544
hgdprs281860544
ensemblrs281860544
gopubmedrs281860544
geneviewrs281860544
scholarrs281860544
googlers281860544
pharmgkbrs281860544
gwascentralrs281860544
openSNPrs281860544
23andMers281860544
23andMe allrs281860544
SNP Nexus

SNPshotrs281860544
SNPdbers281860544
MSV3drs281860544
GWAS Ctlgrs281860544
Max Magnitude0
ClinVar
Risk rs281860544(A;A)
Alt rs281860544(A;A)
Reference rs281860544(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238869C>T
CLNSRC
CLNACC