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: rs798497
rs798497
2 7 2756323 intron variant A/G snv 0.25 0.700 1.000 3 2010 2019
dbSNP: rs798489
rs798489
4 7 2762169 splice donor variant C/T snv 0.20 0.700 1.000 2 2010 2019
dbSNP: rs798544
rs798544
2 7 2723468 intron variant C/T snv 0.25 0.700 1.000 2 2008 2019
dbSNP: rs798554
rs798554
2 7 2720161 intron variant C/T snv 0.25 0.700 1.000 2 2013 2019
dbSNP: rs33932857
rs33932857
1 7 2736084 intron variant G/A snv 0.29 0.700 1.000 1 2017 2017
dbSNP: rs7777484
rs7777484
1 7 2774637 intron variant A/G snv 0.38 0.700 1.000 1 2015 2015
dbSNP: rs798491
rs798491
2 7 2760887 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs798557
rs798557
1 7 2719348 intron variant G/A snv 0.24 0.700 1.000 1 2019 2019