Source: ALL
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: rs505974
rs505974 		4 0.882 0.080 3 190188984 intergenic variant T/C;G snv 0.010 1.000 1 2019 2019
dbSNP: rs79589812
rs79589812
SPATC1L
4 0.882 0.080 21 46181088 intron variant T/A;C snv 0.010 1.000 1 2019 2019