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rs17883986

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17883986(C;T)
Make rs17883986(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944910
GeneHLA-A
is asnp
is mentioned by
dbSNPrs17883986
ebirs17883986
HLIrs17883986
Exacrs17883986
Varsomers17883986
Maprs17883986
PheGenIrs17883986
hapmaprs17883986
1000 genomesrs17883986
hgdprs17883986
ensemblrs17883986
gopubmedrs17883986
geneviewrs17883986
scholarrs17883986
googlers17883986
pharmgkbrs17883986
gwascentralrs17883986
openSNPrs17883986
23andMers17883986
23andMe allrs17883986
SNP Nexus

SNPshotrs17883986
SNPdbers17883986
MSV3drs17883986
GWAS Ctlgrs17883986
GMAF0.1671
Max Magnitude0
ClinVar
Risk rs17883986(T;T)
Alt rs17883986(T;T)
Reference rs17883986(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29912687C>T
CLNSRC
CLNACC