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rs41563719

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41563719(C;G)
Make rs41563719(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942895
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41563719
ebirs41563719
HLIrs41563719
Exacrs41563719
Varsomers41563719
Maprs41563719
PheGenIrs41563719
hapmaprs41563719
1000 genomesrs41563719
hgdprs41563719
ensemblrs41563719
gopubmedrs41563719
geneviewrs41563719
scholarrs41563719
googlers41563719
pharmgkbrs41563719
gwascentralrs41563719
openSNPrs41563719
23andMers41563719
23andMe allrs41563719
SNP Nexus

SNPshotrs41563719
SNPdbers41563719
MSV3drs41563719
GWAS Ctlgrs41563719
Max Magnitude0
ClinVar
Risk rs41563719(G,T;G,T)
Alt rs41563719(G,T;G,T)
Reference rs41563719(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910672C>G; NC_000006.11:g.29910672C>T
CLNSRC
CLNACC