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

rs41554918

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41554918(C;C)
Make rs41554918(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942796
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41554918
ebirs41554918
HLIrs41554918
Exacrs41554918
Varsomers41554918
Maprs41554918
PheGenIrs41554918
hapmaprs41554918
1000 genomesrs41554918
hgdprs41554918
ensemblrs41554918
gopubmedrs41554918
geneviewrs41554918
scholarrs41554918
googlers41554918
pharmgkbrs41554918
gwascentralrs41554918
openSNPrs41554918
23andMers41554918
23andMe allrs41554918
SNP Nexus

SNPshotrs41554918
SNPdbers41554918
MSV3drs41554918
GWAS Ctlgrs41554918
Max Magnitude0
ClinVar
Risk rs41554918(A,C,T;A,C,T)
Alt rs41554918(A,C,T;A,C,T)
Reference rs41554918(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910573G>A; NC_000006.11:g.29910573G>C; NC_000006.11:g.29910573G>T
CLNSRC
CLNACC