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rs199474499

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199474499(A;A)
Make rs199474499(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29943318
GeneHLA-A
is asnp
is mentioned by
dbSNPrs199474499
ebirs199474499
HLIrs199474499
Exacrs199474499
Varsomers199474499
Maprs199474499
PheGenIrs199474499
hapmaprs199474499
1000 genomesrs199474499
hgdprs199474499
ensemblrs199474499
gopubmedrs199474499
geneviewrs199474499
scholarrs199474499
googlers199474499
pharmgkbrs199474499
gwascentralrs199474499
openSNPrs199474499
23andMers199474499
23andMe allrs199474499
SNP Nexus

SNPshotrs199474499
SNPdbers199474499
MSV3drs199474499
GWAS Ctlgrs199474499
Max Magnitude0
ClinVar
Risk rs199474499(A,T;A,T)
Alt rs199474499(A,T;A,T)
Reference rs199474499(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911095C>A; NC_000006.11:g.29911095C>T
CLNSRC
CLNACC