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rs41552817

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41552817(A;A)
Make rs41552817(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271166
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41552817
ebirs41552817
HLIrs41552817
Exacrs41552817
Varsomers41552817
Maprs41552817
PheGenIrs41552817
hapmaprs41552817
1000 genomesrs41552817
hgdprs41552817
ensemblrs41552817
gopubmedrs41552817
geneviewrs41552817
scholarrs41552817
googlers41552817
pharmgkbrs41552817
gwascentralrs41552817
openSNPrs41552817
23andMers41552817
23andMe allrs41552817
SNP Nexus

SNPshotrs41552817
SNPdbers41552817
MSV3drs41552817
GWAS Ctlgrs41552817
GMAF0.02709
Max Magnitude0
ClinVar
Risk rs41552817(A;A)
Alt rs41552817(A;A)
Reference rs41552817(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238943C>T
CLNSRC
CLNACC