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rs281860449

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs281860449(C;C)
Make rs281860449(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271325
GeneHLA-C
is asnp
is mentioned by
dbSNPrs281860449
ebirs281860449
HLIrs281860449
Exacrs281860449
Varsomers281860449
Maprs281860449
PheGenIrs281860449
hapmaprs281860449
1000 genomesrs281860449
hgdprs281860449
ensemblrs281860449
gopubmedrs281860449
geneviewrs281860449
scholarrs281860449
googlers281860449
pharmgkbrs281860449
gwascentralrs281860449
openSNPrs281860449
23andMers281860449
23andMe allrs281860449
SNP Nexus

SNPshotrs281860449
SNPdbers281860449
MSV3drs281860449
GWAS Ctlgrs281860449
Max Magnitude0
ClinVar
Risk rs281860449(C,G;C,G)
Alt rs281860449(C,G;C,G)
Reference rs281860449(T;T)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239102A>C; NC_000006.11:g.31239102A>G
CLNSRC
CLNACC