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: rs1107748
rs1107748
LINC02594
3 1.000 0.080 17 43696446 intron variant T/C snv 0.54 0.010 1.000 1 2018 2018
dbSNP: rs7220711
rs7220711 		2 1.000 0.080 17 43712597 intergenic variant A/G snv 0.52 0.010 1.000 1 2018 2018