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rs41552115

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41552115(C;G)
Make rs41552115(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271079
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41552115
ebirs41552115
HLIrs41552115
Exacrs41552115
Varsomers41552115
Maprs41552115
PheGenIrs41552115
hapmaprs41552115
1000 genomesrs41552115
hgdprs41552115
ensemblrs41552115
gopubmedrs41552115
geneviewrs41552115
scholarrs41552115
googlers41552115
pharmgkbrs41552115
gwascentralrs41552115
openSNPrs41552115
23andMers41552115
23andMe allrs41552115
SNP Nexus

SNPshotrs41552115
SNPdbers41552115
MSV3drs41552115
GWAS Ctlgrs41552115
Max Magnitude0
ClinVar
Risk rs41552115(G,T;G,T)
Alt rs41552115(G,T;G,T)
Reference rs41552115(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238856G>A; NC_000006.11:g.31238856G>C
CLNSRC
CLNACC