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: rs10789752
rs10789752
1 11 110109220 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs661171
rs661171
5 11 110145794 intron variant T/G snv 0.69 0.700 1.000 1 2018 2018
dbSNP: rs689183
rs689183
1 11 110141418 intron variant G/T snv 0.74 0.700 1.000 1 2018 2018
dbSNP: rs746463
rs746463
1 11 110125219 intron variant C/T snv 0.71 0.700 1.000 1 2017 2017