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rs41560912

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41560912(C;C)
Make rs41560912(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943766
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41560912
ebirs41560912
HLIrs41560912
Exacrs41560912
Varsomers41560912
Maprs41560912
PheGenIrs41560912
hapmaprs41560912
1000 genomesrs41560912
hgdprs41560912
ensemblrs41560912
gopubmedrs41560912
geneviewrs41560912
scholarrs41560912
googlers41560912
pharmgkbrs41560912
gwascentralrs41560912
openSNPrs41560912
23andMers41560912
23andMe allrs41560912
SNP Nexus

SNPshotrs41560912
SNPdbers41560912
MSV3drs41560912
GWAS Ctlgrs41560912
Max Magnitude0
ClinVar
Risk rs41560912(C;C)
Alt rs41560912(C;C)
Reference rs41560912(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911543G>C
CLNSRC
CLNACC