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: rs2910200
rs2910200
PTTG1
1 1.000 0.120 5 160422984 non coding transcript exon variant C/T snv 0.23 0.010 1.000 1 2019 2019
dbSNP: rs2981582
rs2981582
FGFR2
21 0.695 0.360 10 121592803 intron variant A/G snv 0.58 0.010 1.000 1 2018 2018