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rs199474477

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199474477(C;G)
Make rs199474477(G;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position29911058
GeneHLA-A
is asnp
is mentioned by
dbSNPrs199474477
ebirs199474477
HLIrs199474477
Exacrs199474477
Varsomers199474477
Maprs199474477
PheGenIrs199474477
hapmaprs199474477
1000 genomesrs199474477
hgdprs199474477
ensemblrs199474477
gopubmedrs199474477
geneviewrs199474477
scholarrs199474477
googlers199474477
pharmgkbrs199474477
gwascentralrs199474477
openSNPrs199474477
23andMers199474477
23andMe allrs199474477
SNP Nexus

SNPshotrs199474477
SNPdbers199474477
MSV3drs199474477
GWAS Ctlgrs199474477
StatusDeleted
Max Magnitude0
ClinVar
Risk rs199474477(G,T;G,T)
Alt rs199474477(G,T;G,T)
Reference rs199474477(C;C)
Significance Histocompatibility
Disease
Variation info
Gene
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911058C>G; NC_000006.11:g.29911058C>T
CLNSRC
CLNACC