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rs17861031

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs17861031(A;A)
Make rs17861031(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position21706706
GenePAX1
is asnp
is mentioned by
dbSNPrs17861031
dbSNP (classic)rs17861031
ClinGenrs17861031
ebirs17861031
HLIrs17861031
Exacrs17861031
Gnomadrs17861031
Varsomers17861031
LitVarrs17861031
Maprs17861031
PheGenIrs17861031
Biobankrs17861031
1000 genomesrs17861031
hgdprs17861031
ensemblrs17861031
geneviewrs17861031
scholarrs17861031
googlers17861031
pharmgkbrs17861031
gwascentralrs17861031
openSNPrs17861031
23andMers17861031
SNPshotrs17861031
SNPdbers17861031
MSV3drs17861031
GWAS Ctlgrs17861031
GMAF0.08035
Max Magnitude0

[PMID 19080705] Fractalkine receptor/ligand genetic variants and carotid intima-media thickness


[PMID 30572100] Genetic polymorphisms of PAX1 are functionally associated with different PUMC types of adolescent idiopathic scoliosis in a northern Chinese Han population.