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

rs41556217

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41556217(C;T)
Make rs41556217(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944244
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41556217
ebirs41556217
HLIrs41556217
Exacrs41556217
Varsomers41556217
Maprs41556217
PheGenIrs41556217
hapmaprs41556217
1000 genomesrs41556217
hgdprs41556217
ensemblrs41556217
gopubmedrs41556217
geneviewrs41556217
scholarrs41556217
googlers41556217
pharmgkbrs41556217
gwascentralrs41556217
openSNPrs41556217
23andMers41556217
23andMe allrs41556217
SNP Nexus

SNPshotrs41556217
SNPdbers41556217
MSV3drs41556217
GWAS Ctlgrs41556217
Max Magnitude0
ClinVar
Risk rs41556217(T;T)
Alt rs41556217(T;T)
Reference rs41556217(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912021C>T
CLNSRC
CLNACC