Rsid Chr Position P value Ref Alt Gwas trait Gene symbol Variant type PMID
rs2027341 chr14 51372606 0.000991 G A Alzheimer's disease PYGL intron 24755620
rs2356535 chr14 51375250 0.000714 G T Alzheimer's disease PYGL intron 24755620
rs10132049 chr14 51376237 0.000369 A G Alzheimer's disease PYGL intron 24755620
rs946617 chr14 51387590 0.0000218 T G Hepatitis B PYGL intron 21750111
rs7142143 chr14 51403531 0.000162 T C Multiple complex diseases PYGL intron 17554300
rs7142143 chr14 51403531 0.000000007 T C Acute lymphoblastic leukemia (childhood) PYGL intron 23007406
rs1890706 chr14 51407580 0.000647 C T Blood pressure,CVD RF and other traits (body mass index (BMI),waist:hip ratio,renin activity in plasma,aldosterone concentration in plasma,BNP levels in plasma,alcohol consumption) PYGL intron 20877124
rs17123244 chr14 51411029 0.000727 A G Type 2 diabetes PYGL cds-synon 17463246
rs111345281 chr14 51411707 0.0000141 C A Sarcoidosis PYGL nearGene-5 22952805