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rs41547916

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41547916(G;G)
Make rs41547916(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942862
GeneHLA-A
is asnp
is mentioned by
dbSNPrs41547916
dbSNP (classic)rs41547916
ClinGenrs41547916
ebirs41547916
HLIrs41547916
Exacrs41547916
Gnomadrs41547916
Varsomers41547916
LitVarrs41547916
Maprs41547916
PheGenIrs41547916
Biobankrs41547916
1000 genomesrs41547916
hgdprs41547916
ensemblrs41547916
geneviewrs41547916
scholarrs41547916
googlers41547916
pharmgkbrs41547916
gwascentralrs41547916
openSNPrs41547916
23andMers41547916
SNPshotrs41547916
SNPdbers41547916
MSV3drs41547916
GWAS Ctlgrs41547916
Max Magnitude0
ClinVar
Risk rs41547916(C;C) rs41547916(G;G)
Alt rs41547916(C;C) rs41547916(G;G)
Reference Rs41547916(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910639T>C; NC_000006.11:g.29910639T>G
CLNSRC
CLNACC