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rs17885212

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs17885212(A;A)
Make rs17885212(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position29944103
GeneHLA-A
is asnp
is mentioned by
dbSNPrs17885212
ebirs17885212
HLIrs17885212
Exacrs17885212
Varsomers17885212
Maprs17885212
PheGenIrs17885212
hapmaprs17885212
1000 genomesrs17885212
hgdprs17885212
ensemblrs17885212
gopubmedrs17885212
geneviewrs17885212
scholarrs17885212
googlers17885212
pharmgkbrs17885212
gwascentralrs17885212
openSNPrs17885212
23andMers17885212
23andMe allrs17885212
SNP Nexus

SNPshotrs17885212
SNPdbers17885212
MSV3drs17885212
GWAS Ctlgrs17885212
Max Magnitude0
ClinVar
Risk rs17885212(A;A)
Alt rs17885212(A;A)
Reference rs17885212(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-A
CLNDBN
Reversed 0
HGVS NC_000006.11:g.29911880T>A
CLNSRC
CLNACC