Have questions? Visit https://www.reddit.com/r/SNPedia

rs1071742

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1071742(C;C)
Make rs1071742(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942982
GeneHLA-A
is asnp
is mentioned by
dbSNPrs1071742
ebirs1071742
HLIrs1071742
Exacrs1071742
Varsomers1071742
Maprs1071742
PheGenIrs1071742
hapmaprs1071742
1000 genomesrs1071742
hgdprs1071742
ensemblrs1071742
gopubmedrs1071742
geneviewrs1071742
scholarrs1071742
googlers1071742
pharmgkbrs1071742
gwascentralrs1071742
openSNPrs1071742
23andMers1071742
23andMe allrs1071742
SNP Nexus

SNPshotrs1071742
SNPdbers1071742
MSV3drs1071742
GWAS Ctlgrs1071742
GMAF0.1579
Max Magnitude0
ClinVar
Risk rs1071742(A,C,G;A,C,G)
Alt rs1071742(A,C,G;A,C,G)
Reference rs1071742(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910759T; NC_000006.11:g.29910759T>A; NC_000006.11:g.29910759T>C; NC_000006.11:g.29910759T>G
CLNSRC
CLNACC


GET Evidence
HLA-A-VD100EN
aa_change ValAsp100GluAsn
aa_change_short VD100EN
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0930233
summary