PVT1, Pvt1 oncogene, 5820

N. diseases: 27; N. variants: 31
Disease: Birth Weight ×
Source: GWASCAT ×
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2608029
rs2608029 		1.000 0.040 8 128157880 intron variant C/G snv 0.37
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2019 2019