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rs1071743

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1071743(A;C)
Make rs1071743(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943279
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1071743
ebirs1071743
HLIrs1071743
Exacrs1071743
Varsomers1071743
Maprs1071743
PheGenIrs1071743
hapmaprs1071743
1000 genomesrs1071743
hgdprs1071743
ensemblrs1071743
gopubmedrs1071743
geneviewrs1071743
scholarrs1071743
googlers1071743
pharmgkbrs1071743
gwascentralrs1071743
openSNPrs1071743
23andMers1071743
23andMe allrs1071743
SNP Nexus

SNPshotrs1071743
SNPdbers1071743
MSV3drs1071743
GWAS Ctlgrs1071743
GMAF0.1956
Max Magnitude0
ClinVar
Risk rs1071743(C,G,T;C,G,T)
Alt rs1071743(C,G,T;C,G,T)
Reference rs1071743(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911056A>C; NC_000006.11:g.29911056A>G; NC_000006.11:g.29911056A>T
CLNSRC
CLNACC


GET Evidence
HLA-A-I119L
aa_change Ile119Leu
aa_change_short I119L
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.14529
summary