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rs199474417

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199474417(C;C)
Make rs199474417(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942930
GeneHLA-A
is asnp
is mentioned by
dbSNPrs199474417
ebirs199474417
HLIrs199474417
Exacrs199474417
Varsomers199474417
Maprs199474417
PheGenIrs199474417
hapmaprs199474417
1000 genomesrs199474417
hgdprs199474417
ensemblrs199474417
gopubmedrs199474417
geneviewrs199474417
scholarrs199474417
googlers199474417
pharmgkbrs199474417
gwascentralrs199474417
openSNPrs199474417
23andMers199474417
23andMe allrs199474417
SNP Nexus

SNPshotrs199474417
SNPdbers199474417
MSV3drs199474417
GWAS Ctlgrs199474417
Max Magnitude0
ClinVar
Risk rs199474417(C;C)
Alt rs199474417(C;C)
Reference rs199474417(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910707T>C
CLNSRC
CLNACC