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

rs41561213

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41561213(A;G)
Make rs41561213(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271094
GeneHLA-C
is asnp
is mentioned by
dbSNPrs41561213
ebirs41561213
HLIrs41561213
Exacrs41561213
Varsomers41561213
Maprs41561213
PheGenIrs41561213
hapmaprs41561213
1000 genomesrs41561213
hgdprs41561213
ensemblrs41561213
gopubmedrs41561213
geneviewrs41561213
scholarrs41561213
googlers41561213
pharmgkbrs41561213
gwascentralrs41561213
openSNPrs41561213
23andMers41561213
23andMe allrs41561213
SNP Nexus

SNPshotrs41561213
SNPdbers41561213
MSV3drs41561213
GWAS Ctlgrs41561213
Max Magnitude0
ClinVar
Risk rs41561213(G;G)
Alt rs41561213(G;G)
Reference rs41561213(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31238871T>C
CLNSRC
CLNACC