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rs41544012

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41544012(A;G)
Make rs41544012(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942911
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41544012
ebirs41544012
HLIrs41544012
Exacrs41544012
Varsomers41544012
Maprs41544012
PheGenIrs41544012
hapmaprs41544012
1000 genomesrs41544012
hgdprs41544012
ensemblrs41544012
gopubmedrs41544012
geneviewrs41544012
scholarrs41544012
googlers41544012
pharmgkbrs41544012
gwascentralrs41544012
openSNPrs41544012
23andMers41544012
23andMe allrs41544012
SNP Nexus

SNPshotrs41544012
SNPdbers41544012
MSV3drs41544012
GWAS Ctlgrs41544012
GMAF0.1212
Max Magnitude0
ClinVar
Risk rs41544012(G;G)
Alt rs41544012(G;G)
Reference rs41544012(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910688A>G
CLNSRC
CLNACC


GET Evidence
HLA-A-I76M
aa_change Ile76Met
aa_change_short I76M
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0584077
summary