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rs2308592

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2308592(G;T)
Make rs2308592(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271152
GeneHLA-C
is asnp
is mentioned by
dbSNPrs2308592
ebirs2308592
HLIrs2308592
Exacrs2308592
Varsomers2308592
Maprs2308592
PheGenIrs2308592
hapmaprs2308592
1000 genomesrs2308592
hgdprs2308592
ensemblrs2308592
gopubmedrs2308592
geneviewrs2308592
scholarrs2308592
googlers2308592
pharmgkbrs2308592
gwascentralrs2308592
openSNPrs2308592
23andMers2308592
23andMe allrs2308592
SNP Nexus

SNPshotrs2308592
SNPdbers2308592
MSV3drs2308592
GWAS Ctlgrs2308592
Max Magnitude0
ClinVar
Risk rs2308592(A,C,T;A,C,T)
Alt rs2308592(A,C,T;A,C,T)
Reference rs2308592(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238929C>G; NC_000006.11:g.31238929C>T
CLNSRC
CLNACC