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rs41545116

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41545116(A;A)
Make rs41545116(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942789
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41545116
ebirs41545116
HLIrs41545116
Exacrs41545116
Varsomers41545116
Maprs41545116
PheGenIrs41545116
hapmaprs41545116
1000 genomesrs41545116
hgdprs41545116
ensemblrs41545116
gopubmedrs41545116
geneviewrs41545116
scholarrs41545116
googlers41545116
pharmgkbrs41545116
gwascentralrs41545116
openSNPrs41545116
23andMers41545116
23andMe allrs41545116
SNP Nexus

SNPshotrs41545116
SNPdbers41545116
MSV3drs41545116
GWAS Ctlgrs41545116
Max Magnitude0
ClinVar
Risk rs41545116(A,C;A,C)
Alt rs41545116(A,C;A,C)
Reference rs41545116(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910566G>A; NC_000006.11:g.29910566G>C
CLNSRC
CLNACC


GET Evidence
HLA-A-V36M
aa_change Val36Met
aa_change_short V36M
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0128133
summary