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rs41551117

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41551117(A;A)
Make rs41551117(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943521
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41551117
ebirs41551117
HLIrs41551117
Exacrs41551117
Varsomers41551117
Maprs41551117
PheGenIrs41551117
hapmaprs41551117
1000 genomesrs41551117
hgdprs41551117
ensemblrs41551117
gopubmedrs41551117
geneviewrs41551117
scholarrs41551117
googlers41551117
pharmgkbrs41551117
gwascentralrs41551117
openSNPrs41551117
23andMers41551117
23andMe allrs41551117
SNP Nexus

SNPshotrs41551117
SNPdbers41551117
MSV3drs41551117
GWAS Ctlgrs41551117
Max Magnitude0
ClinVar
Risk rs41551117(A,T;A,T)
Alt rs41551117(A,T;A,T)
Reference rs41551117(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911298G>A; NC_000006.11:g.29911298G>T
CLNSRC
CLNACC