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rs281860568

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860568(A;A)
Make rs281860568(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270318
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860568
ebirs281860568
HLIrs281860568
Exacrs281860568
Varsomers281860568
Maprs281860568
PheGenIrs281860568
hapmaprs281860568
1000 genomesrs281860568
hgdprs281860568
ensemblrs281860568
gopubmedrs281860568
geneviewrs281860568
scholarrs281860568
googlers281860568
pharmgkbrs281860568
gwascentralrs281860568
openSNPrs281860568
23andMers281860568
23andMe allrs281860568
SNP Nexus

SNPshotrs281860568
SNPdbers281860568
MSV3drs281860568
GWAS Ctlgrs281860568
Max Magnitude0
ClinVar
Risk rs281860568(A;A)
Alt rs281860568(A;A)
Reference rs281860568(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238095C>T
CLNSRC
CLNACC