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rs41563116

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41563116(C;C)
Make rs41563116(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943507
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41563116
ebirs41563116
HLIrs41563116
Exacrs41563116
Varsomers41563116
Maprs41563116
PheGenIrs41563116
hapmaprs41563116
1000 genomesrs41563116
hgdprs41563116
ensemblrs41563116
gopubmedrs41563116
geneviewrs41563116
scholarrs41563116
googlers41563116
pharmgkbrs41563116
gwascentralrs41563116
openSNPrs41563116
23andMers41563116
23andMe allrs41563116
SNP Nexus

SNPshotrs41563116
SNPdbers41563116
MSV3drs41563116
GWAS Ctlgrs41563116
Max Magnitude0
ClinVar
Risk rs41563116(A,C;A,C)
Alt rs41563116(A,C;A,C)
Reference rs41563116(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911284T>A; NC_000006.11:g.29911284T>C
CLNSRC
CLNACC