Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs17726276
rs17726276
1 19 40785214 intron variant G/A snv 0.42 0.700 1.000 1 2018 2018
dbSNP: rs2233154
rs2233154
1 19 40775441 intron variant C/T snv 0.10 0.700 1.000 1 2018 2018