RS1551570 PPAN

Health Risk Chr 19:10107353 snv intron variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[GWAS:Narcolepsy]
Associated Conditions
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Narcolepsy OR: 1.32 4E-10 PubMed
Population Frequencies
gnomAD ALL
0%
1kG AFR
63.2%
1kG ALL
33.4%
1kG AMR
69.3%
1kG EAS
29.5%
1kG EUR
40.4%
1kG SAS
72.1%
Ask Dr. Hemsworth about this variant