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rs41562120

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41562120(A;A)
Make rs41562120(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943489
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41562120
ebirs41562120
HLIrs41562120
Exacrs41562120
Varsomers41562120
Maprs41562120
PheGenIrs41562120
hapmaprs41562120
1000 genomesrs41562120
hgdprs41562120
ensemblrs41562120
gopubmedrs41562120
geneviewrs41562120
scholarrs41562120
googlers41562120
pharmgkbrs41562120
gwascentralrs41562120
openSNPrs41562120
23andMers41562120
23andMe allrs41562120
SNP Nexus

SNPshotrs41562120
SNPdbers41562120
MSV3drs41562120
GWAS Ctlgrs41562120
Max Magnitude0
ClinVar
Risk rs41562120(A,C,T;A,C,T)
Alt rs41562120(A,C,T;A,C,T)
Reference rs41562120(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911266G>A; NC_000006.11:g.29911266G>C; NC_000006.11:g.29911266G>T
CLNSRC
CLNACC