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: rs925488
rs925488
PTCSC2
2 1.000 0.040 9 97784109 intron variant G/A snv 0.71 0.700 1.000 1 2018 2018
dbSNP: rs9355610
rs9355610
LOC105378120
3 0.882 0.200 6 166969587 downstream gene variant G/A;T snv 0.010 1.000 1 2018 2018