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

rs41556016

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41556016(A;A)
Make rs41556016(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943344
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41556016
ebirs41556016
HLIrs41556016
Exacrs41556016
Varsomers41556016
Maprs41556016
PheGenIrs41556016
hapmaprs41556016
1000 genomesrs41556016
hgdprs41556016
ensemblrs41556016
gopubmedrs41556016
geneviewrs41556016
scholarrs41556016
googlers41556016
pharmgkbrs41556016
gwascentralrs41556016
openSNPrs41556016
23andMers41556016
23andMe allrs41556016
SNP Nexus

SNPshotrs41556016
SNPdbers41556016
MSV3drs41556016
GWAS Ctlgrs41556016
Max Magnitude0
ClinVar
Risk rs41556016(A,G,T;A,G,T)
Alt rs41556016(A,G,T;A,G,T)
Reference rs41556016(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911121C>A; NC_000006.11:g.29911121C>G; NC_000006.11:g.29911121C>T
CLNSRC
CLNACC