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rs41557118

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41557118(A;A)
Make rs41557118(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943316
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41557118
ebirs41557118
HLIrs41557118
Exacrs41557118
Varsomers41557118
Maprs41557118
PheGenIrs41557118
hapmaprs41557118
1000 genomesrs41557118
hgdprs41557118
ensemblrs41557118
gopubmedrs41557118
geneviewrs41557118
scholarrs41557118
googlers41557118
pharmgkbrs41557118
gwascentralrs41557118
openSNPrs41557118
23andMers41557118
23andMe allrs41557118
SNP Nexus

SNPshotrs41557118
SNPdbers41557118
MSV3drs41557118
GWAS Ctlgrs41557118
Max Magnitude0
ClinVar
Risk rs41557118(A,C,T;A,C,T)
Alt rs41557118(A,C,T;A,C,T)
Reference rs41557118(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911093G>A; NC_000006.11:g.29911093G>C; NC_000006.11:g.29911093G>T
CLNSRC
CLNACC