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rs41548812

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41548812(A;A)
Make rs41548812(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943328
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41548812
ebirs41548812
HLIrs41548812
Exacrs41548812
Varsomers41548812
Maprs41548812
PheGenIrs41548812
hapmaprs41548812
1000 genomesrs41548812
hgdprs41548812
ensemblrs41548812
gopubmedrs41548812
geneviewrs41548812
scholarrs41548812
googlers41548812
pharmgkbrs41548812
gwascentralrs41548812
openSNPrs41548812
23andMers41548812
23andMe allrs41548812
SNP Nexus

SNPshotrs41548812
SNPdbers41548812
MSV3drs41548812
GWAS Ctlgrs41548812
Max Magnitude0
ClinVar
Risk rs41548812(A,C;A,C)
Alt rs41548812(A,C;A,C)
Reference rs41548812(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911105G>A; NC_000006.11:g.29911105G>C
CLNSRC
CLNACC