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rs41557315

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41557315(A;G)
Make rs41557315(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944131
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41557315
ebirs41557315
HLIrs41557315
Exacrs41557315
Varsomers41557315
Maprs41557315
PheGenIrs41557315
hapmaprs41557315
1000 genomesrs41557315
hgdprs41557315
ensemblrs41557315
gopubmedrs41557315
geneviewrs41557315
scholarrs41557315
googlers41557315
pharmgkbrs41557315
gwascentralrs41557315
openSNPrs41557315
23andMers41557315
23andMe allrs41557315
SNP Nexus

SNPshotrs41557315
SNPdbers41557315
MSV3drs41557315
GWAS Ctlgrs41557315
Max Magnitude0
ClinVar
Risk rs41557315(G;G)
Alt rs41557315(G;G)
Reference rs41557315(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911908A>G
CLNSRC
CLNACC


GET Evidence
HLA-A-K210R
aa_change Lys210Arg
aa_change_short K210R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.00892857
summary