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rs41564012

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41564012(A;A)
Make rs41564012(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942620
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41564012
ebirs41564012
HLIrs41564012
Exacrs41564012
Varsomers41564012
Maprs41564012
PheGenIrs41564012
hapmaprs41564012
1000 genomesrs41564012
hgdprs41564012
ensemblrs41564012
gopubmedrs41564012
geneviewrs41564012
scholarrs41564012
googlers41564012
pharmgkbrs41564012
gwascentralrs41564012
openSNPrs41564012
23andMers41564012
23andMe allrs41564012
SNP Nexus

SNPshotrs41564012
SNPdbers41564012
MSV3drs41564012
GWAS Ctlgrs41564012
GMAF0.01653
Max Magnitude0
ClinVar
Risk rs41564012(A;A)
Alt rs41564012(A;A)
Reference rs41564012(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910397T>A
CLNSRC
CLNACC


GET Evidence
HLA-A-W23R
aa_change Trp23Arg
aa_change_short W23R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0198324
summary