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rs281860416

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281860416(A;A)
Make rs281860416(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271634
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860416
ebirs281860416
HLIrs281860416
Exacrs281860416
Varsomers281860416
Maprs281860416
PheGenIrs281860416
hapmaprs281860416
1000 genomesrs281860416
hgdprs281860416
ensemblrs281860416
gopubmedrs281860416
geneviewrs281860416
scholarrs281860416
googlers281860416
pharmgkbrs281860416
gwascentralrs281860416
openSNPrs281860416
23andMers281860416
23andMe allrs281860416
SNP Nexus

SNPshotrs281860416
SNPdbers281860416
MSV3drs281860416
GWAS Ctlgrs281860416
Max Magnitude0
ClinVar
Risk rs281860416(A,C;A,C)
Alt rs281860416(A,C;A,C)
Reference rs281860416(G;G)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239411C>G; NC_000006.11:g.31239411C>T
CLNSRC
CLNACC