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rs41560913

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41560913(A;A)
Make rs41560913(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942924
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41560913
ebirs41560913
HLIrs41560913
Exacrs41560913
Varsomers41560913
Maprs41560913
PheGenIrs41560913
hapmaprs41560913
1000 genomesrs41560913
hgdprs41560913
ensemblrs41560913
gopubmedrs41560913
geneviewrs41560913
scholarrs41560913
googlers41560913
pharmgkbrs41560913
gwascentralrs41560913
openSNPrs41560913
23andMers41560913
23andMe allrs41560913
SNP Nexus

SNPshotrs41560913
SNPdbers41560913
MSV3drs41560913
GWAS Ctlgrs41560913
Max Magnitude0
ClinVar
Risk rs41560913(A,G,T;A,G,T)
Alt rs41560913(A,G,T;A,G,T)
Reference rs41560913(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910701C>A; NC_000006.11:g.29910701C>G; NC_000006.11:g.29910701C>T
CLNSRC
CLNACC