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rs2001181

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2001181(C;T)
Make rs2001181(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269221
GeneHLA-C
is asnp
is mentioned by
dbSNPrs2001181
ebirs2001181
HLIrs2001181
Exacrs2001181
Varsomers2001181
Maprs2001181
PheGenIrs2001181
hapmaprs2001181
1000 genomesrs2001181
hgdprs2001181
ensemblrs2001181
gopubmedrs2001181
geneviewrs2001181
scholarrs2001181
googlers2001181
pharmgkbrs2001181
gwascentralrs2001181
openSNPrs2001181
23andMers2001181
23andMe allrs2001181
SNP Nexus

SNPshotrs2001181
SNPdbers2001181
MSV3drs2001181
GWAS Ctlgrs2001181
GMAF0.1281
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs2001181(T;T)
Alt rs2001181(T;T)
Reference rs2001181(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31236998C; NC_000006.11:g.31236998C>T
CLNSRC
CLNACC