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: rs13010010
rs13010010
1 2 100236272 intron variant C/T snv 0.27 0.700 1.000 4 2017 2019
dbSNP: rs10865035
rs10865035
2 1.000 0.080 2 100219272 intron variant A/G snv 0.42 0.700 1.000 1 2018 2018
dbSNP: rs9653442
rs9653442
2 1.000 0.120 2 100208905 intron variant C/T snv 0.46 0.700 1.000 1 2019 2019