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rs17885299

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs17885299(C;C)
Make rs17885299(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position29942673
GeneHLA-A
is asnp
is mentioned by
dbSNPrs17885299
ebirs17885299
HLIrs17885299
Exacrs17885299
Varsomers17885299
Maprs17885299
PheGenIrs17885299
hapmaprs17885299
1000 genomesrs17885299
hgdprs17885299
ensemblrs17885299
gopubmedrs17885299
geneviewrs17885299
scholarrs17885299
googlers17885299
pharmgkbrs17885299
gwascentralrs17885299
openSNPrs17885299
23andMers17885299
23andMe allrs17885299
SNP Nexus

SNPshotrs17885299
SNPdbers17885299
MSV3drs17885299
GWAS Ctlgrs17885299
GMAF0.2374
Max Magnitude0
ClinVar
Risk rs17885299(C;C)
Alt rs17885299(C;C)
Reference rs17885299(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29910450G>C
CLNSRC
CLNACC