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

rs2075684

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2075684(A;G)
Make rs2075684(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942781
GeneHLA-A
is asnp
is mentioned by
dbSNPrs2075684
ebirs2075684
HLIrs2075684
Exacrs2075684
Varsomers2075684
Maprs2075684
PheGenIrs2075684
hapmaprs2075684
1000 genomesrs2075684
hgdprs2075684
ensemblrs2075684
gopubmedrs2075684
geneviewrs2075684
scholarrs2075684
googlers2075684
pharmgkbrs2075684
gwascentralrs2075684
openSNPrs2075684
23andMers2075684
23andMe allrs2075684
SNP Nexus

SNPshotrs2075684
SNPdbers2075684
MSV3drs2075684
GWAS Ctlgrs2075684
GMAF0.4495
Max Magnitude0
ClinVar
Risk rs2075684(G;G) rs2075684(T;T)
Alt rs2075684(G;G) rs2075684(T;T)
Reference Rs2075684(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 1
HGVS NC_000006.11:g.29910558T>A; NC_000006.11:g.29910558T>C
CLNSRC
CLNACC


GET Evidence
HLA-A-F33Y
aa_change Phe33Tyr
aa_change_short F33Y
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.211864
summary