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rs41563419

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41563419(C;C)
Make rs41563419(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944270
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41563419
ebirs41563419
HLIrs41563419
Exacrs41563419
Varsomers41563419
Maprs41563419
PheGenIrs41563419
hapmaprs41563419
1000 genomesrs41563419
hgdprs41563419
ensemblrs41563419
gopubmedrs41563419
geneviewrs41563419
scholarrs41563419
googlers41563419
pharmgkbrs41563419
gwascentralrs41563419
openSNPrs41563419
23andMers41563419
23andMe allrs41563419
SNP Nexus

SNPshotrs41563419
SNPdbers41563419
MSV3drs41563419
GWAS Ctlgrs41563419
Max Magnitude0
ClinVar
Risk rs41563419(C,T;C,T)
Alt rs41563419(C,T;C,T)
Reference rs41563419(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912047G>C; NC_000006.11:g.29912047G>T
CLNSRC
CLNACC