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: rs12906125
rs12906125
FES
1 15 90884382 intron variant G/A snv 0.29 0.700 1.000 1 2016 2016
dbSNP: rs4932373
rs4932373
FES
2 1.000 0.040 15 90886057 intron variant A/C snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs7183988
rs7183988
FES
1 15 90885359 missense variant T/G snv 0.59 0.53 0.700 1.000 1 2019 2019