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rs41563718

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41563718(C;G)
Make rs41563718(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943326
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41563718
ebirs41563718
HLIrs41563718
Exacrs41563718
Varsomers41563718
Maprs41563718
PheGenIrs41563718
hapmaprs41563718
1000 genomesrs41563718
hgdprs41563718
ensemblrs41563718
gopubmedrs41563718
geneviewrs41563718
scholarrs41563718
googlers41563718
pharmgkbrs41563718
gwascentralrs41563718
openSNPrs41563718
23andMers41563718
23andMe allrs41563718
SNP Nexus

SNPshotrs41563718
SNPdbers41563718
MSV3drs41563718
GWAS Ctlgrs41563718
GMAF0.01791
Max Magnitude0
ClinVar
Risk rs41563718(A,G,T;A,G,T)
Alt rs41563718(A,G,T;A,G,T)
Reference rs41563718(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911103C>A; NC_000006.11:g.29911103C>G; NC_000006.11:g.29911103C>T
CLNSRC
CLNACC