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

rs41541518

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41541518(C;G)
Make rs41541518(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943417
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41541518
ebirs41541518
HLIrs41541518
Exacrs41541518
Varsomers41541518
Maprs41541518
PheGenIrs41541518
hapmaprs41541518
1000 genomesrs41541518
hgdprs41541518
ensemblrs41541518
gopubmedrs41541518
geneviewrs41541518
scholarrs41541518
googlers41541518
pharmgkbrs41541518
gwascentralrs41541518
openSNPrs41541518
23andMers41541518
23andMe allrs41541518
SNP Nexus

SNPshotrs41541518
SNPdbers41541518
MSV3drs41541518
GWAS Ctlgrs41541518
Max Magnitude0
ClinVar
Risk rs41541518(G,T;G,T)
Alt rs41541518(G,T;G,T)
Reference rs41541518(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911194C>G; NC_000006.11:g.29911194C>T
CLNSRC
CLNACC