SPATA18, spermatogenesis associated 18, 132671

N. diseases: 13; N. variants: 1
Source: ALL
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: rs3113509
rs3113509 		4 52066659 intron variant C/T snv 0.58
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019