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rs41548117

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41548117(-;-)
Make rs41548117(-;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31269324
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41548117
ebirs41548117
HLIrs41548117
Exacrs41548117
Varsomers41548117
Maprs41548117
PheGenIrs41548117
hapmaprs41548117
1000 genomesrs41548117
hgdprs41548117
ensemblrs41548117
gopubmedrs41548117
geneviewrs41548117
scholarrs41548117
googlers41548117
pharmgkbrs41548117
gwascentralrs41548117
openSNPrs41548117
23andMers41548117
23andMe allrs41548117
SNP Nexus

SNPshotrs41548117
SNPdbers41548117
MSV3drs41548117
GWAS Ctlgrs41548117
GMAF0.03444
Max Magnitude0
ClinVar
Risk rs41548117(;)
Alt rs41548117(;)
Reference rs41548117(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31237101delC
CLNSRC
CLNACC