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rs41563617

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41563617(A;A)
Make rs41563617(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943022
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41563617
ebirs41563617
HLIrs41563617
Exacrs41563617
Varsomers41563617
Maprs41563617
PheGenIrs41563617
hapmaprs41563617
1000 genomesrs41563617
hgdprs41563617
ensemblrs41563617
gopubmedrs41563617
geneviewrs41563617
scholarrs41563617
googlers41563617
pharmgkbrs41563617
gwascentralrs41563617
openSNPrs41563617
23andMers41563617
23andMe allrs41563617
SNP Nexus

SNPshotrs41563617
SNPdbers41563617
MSV3drs41563617
GWAS Ctlgrs41563617
Max Magnitude0
ClinVar
Risk rs41563617(A;A)
Alt rs41563617(A;A)
Reference rs41563617(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910799G>A
CLNSRC
CLNACC