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: rs1496255
rs1496255 		4 4 120683279 downstream gene variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs41434646
rs41434646
LOC102724340 ; LOC105373776
3 2 184295785 intron variant A/C;G snv 4.7E-03 0.700 1.000 1 2017 2017
dbSNP: rs9833533
rs9833533
FHIT
2 3 60582520 intron variant G/A snv 8.3E-02 0.700 1.000 1 2017 2017