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

rs41551921

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41551921(A;A)
Make rs41551921(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943466
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41551921
dbSNP (classic)rs41551921
ClinGenrs41551921
ebirs41551921
HLIrs41551921
Exacrs41551921
Gnomadrs41551921
Varsomers41551921
LitVarrs41551921
Maprs41551921
PheGenIrs41551921
Biobankrs41551921
1000 genomesrs41551921
hgdprs41551921
ensemblrs41551921
geneviewrs41551921
scholarrs41551921
googlers41551921
pharmgkbrs41551921
gwascentralrs41551921
openSNPrs41551921
23andMers41551921
SNPshotrs41551921
SNPdbers41551921
MSV3drs41551921
GWAS Ctlgrs41551921
Max Magnitude0
ClinVar
Risk rs41551921(A;A) rs41551921(C;C)
Alt rs41551921(A;A) rs41551921(C;C)
Reference Rs41551921(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911243G>A; NC_000006.11:g.29911243G>C
CLNSRC
CLNACC