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: rs17107315
rs17107315
40 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.750 1.000 7 2002 2009
dbSNP: rs148954387
rs148954387
3 0.882 0.080 5 147828020 splice donor variant A/G;T snv 3.1E-04 0.700 0