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rs17887246

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs17887246(C;C)
Make rs17887246(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944872
GeneHLA-A
is asnp
is mentioned by
dbSNPrs17887246
ebirs17887246
HLIrs17887246
Exacrs17887246
Varsomers17887246
Maprs17887246
PheGenIrs17887246
hapmaprs17887246
1000 genomesrs17887246
hgdprs17887246
ensemblrs17887246
gopubmedrs17887246
geneviewrs17887246
scholarrs17887246
googlers17887246
pharmgkbrs17887246
gwascentralrs17887246
openSNPrs17887246
23andMers17887246
23andMe allrs17887246
SNP Nexus

SNPshotrs17887246
SNPdbers17887246
MSV3drs17887246
GWAS Ctlgrs17887246
Max Magnitude0
ClinVar
Risk rs17887246(C;C)
Alt rs17887246(C;C)
Reference rs17887246(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912649G>C
CLNSRC
CLNACC