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rs41554316

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41554316(A;C)
Make rs41554316(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944538
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41554316
ebirs41554316
HLIrs41554316
Exacrs41554316
Varsomers41554316
Maprs41554316
PheGenIrs41554316
hapmaprs41554316
1000 genomesrs41554316
hgdprs41554316
ensemblrs41554316
gopubmedrs41554316
geneviewrs41554316
scholarrs41554316
googlers41554316
pharmgkbrs41554316
gwascentralrs41554316
openSNPrs41554316
23andMers41554316
23andMe allrs41554316
SNP Nexus

SNPshotrs41554316
SNPdbers41554316
MSV3drs41554316
GWAS Ctlgrs41554316
GMAF0.1267
Max Magnitude0
ClinVar
Risk rs41554316(C;C)
Alt rs41554316(C;C)
Reference rs41554316(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912315A>C
CLNSRC
CLNACC


GET Evidence
HLA-A-I312V
aa_change Ile312Val
aa_change_short I312V
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0125
summary