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rs41560917

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41560917(A;A)
Make rs41560917(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943323
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41560917
dbSNP (classic)rs41560917
ClinGenrs41560917
ebirs41560917
HLIrs41560917
Exacrs41560917
Gnomadrs41560917
Varsomers41560917
LitVarrs41560917
Maprs41560917
PheGenIrs41560917
Biobankrs41560917
1000 genomesrs41560917
hgdprs41560917
ensemblrs41560917
geneviewrs41560917
scholarrs41560917
googlers41560917
pharmgkbrs41560917
gwascentralrs41560917
openSNPrs41560917
23andMers41560917
SNPshotrs41560917
SNPdbers41560917
MSV3drs41560917
GWAS Ctlgrs41560917
Max Magnitude0
ClinVar
Risk rs41560917(A;A)
Alt rs41560917(A;A)
Reference Rs41560917(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911100C>A
CLNSRC
CLNACC