Have questions? Visit https://www.reddit.com/r/SNPedia

rs41552317

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41552317(C;C)
Make rs41552317(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942991
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41552317
ebirs41552317
HLIrs41552317
Exacrs41552317
Varsomers41552317
Maprs41552317
PheGenIrs41552317
hapmaprs41552317
1000 genomesrs41552317
hgdprs41552317
ensemblrs41552317
gopubmedrs41552317
geneviewrs41552317
scholarrs41552317
googlers41552317
pharmgkbrs41552317
gwascentralrs41552317
openSNPrs41552317
23andMers41552317
23andMe allrs41552317
SNP Nexus

SNPshotrs41552317
SNPdbers41552317
MSV3drs41552317
GWAS Ctlgrs41552317
GMAF0.001837
Max Magnitude0
ClinVar
Risk rs41552317(A,C;A,C)
Alt rs41552317(A,C;A,C)
Reference rs41552317(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910768G>A; NC_000006.11:g.29910768G>C
CLNSRC
CLNACC