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rs1059896

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1059896(A;A)
Make rs1059896(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944565
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1059896
ebirs1059896
HLIrs1059896
Exacrs1059896
Varsomers1059896
Maprs1059896
PheGenIrs1059896
hapmaprs1059896
1000 genomesrs1059896
hgdprs1059896
ensemblrs1059896
gopubmedrs1059896
geneviewrs1059896
scholarrs1059896
googlers1059896
pharmgkbrs1059896
gwascentralrs1059896
openSNPrs1059896
23andMers1059896
23andMe allrs1059896
SNP Nexus

SNPshotrs1059896
SNPdbers1059896
MSV3drs1059896
GWAS Ctlgrs1059896
Max Magnitude0
ClinVar
Risk rs1059896(A;A)
Alt rs1059896(A;A)
Reference rs1059896(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912342G>A
CLNSRC
CLNACC


GET Evidence
HLA-A-V321M
aa_change Val321Met
aa_change_short V321M
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.00132908
summary