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rs1059423

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1059423(A;A)
Make rs1059423(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942804
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059423
ebirs1059423
HLIrs1059423
Exacrs1059423
Varsomers1059423
Maprs1059423
PheGenIrs1059423
hapmaprs1059423
1000 genomesrs1059423
hgdprs1059423
ensemblrs1059423
gopubmedrs1059423
geneviewrs1059423
scholarrs1059423
googlers1059423
pharmgkbrs1059423
gwascentralrs1059423
openSNPrs1059423
23andMers1059423
23andMe allrs1059423
SNP Nexus

SNPshotrs1059423
SNPdbers1059423
MSV3drs1059423
GWAS Ctlgrs1059423
GMAF0.1097
Max Magnitude0
ClinVar
Risk rs1059423(A,T;A,T)
Alt rs1059423(A,T;A,T)
Reference rs1059423(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910581C>A; NC_000006.11:g.29910581C>T
CLNSRC
CLNACC


GET Evidence
HLA-A-R41S
aa_change Arg41Ser
aa_change_short R41S
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.062535
summary