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rs41559418

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41559418(A;A)
Make rs41559418(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31270427
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41559418
ebirs41559418
HLIrs41559418
Exacrs41559418
Varsomers41559418
Maprs41559418
PheGenIrs41559418
hapmaprs41559418
1000 genomesrs41559418
hgdprs41559418
ensemblrs41559418
gopubmedrs41559418
geneviewrs41559418
scholarrs41559418
googlers41559418
pharmgkbrs41559418
gwascentralrs41559418
openSNPrs41559418
23andMers41559418
23andMe allrs41559418
SNP Nexus

SNPshotrs41559418
SNPdbers41559418
MSV3drs41559418
GWAS Ctlgrs41559418
Max Magnitude0
ClinVar
Risk rs41559418(A;A)
Alt rs41559418(A;A)
Reference rs41559418(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238204C>T
CLNSRC
CLNACC