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: rs10922478
rs10922478
1 1 88678370 intron variant A/G snv 0.61 0.700 1.000 1 2019 2019
dbSNP: rs1498911
rs1498911
1 1 88519949 intron variant A/C snv 0.39 0.700 1.000 1 2017 2017
dbSNP: rs4411112
rs4411112
1 1 88141933 intron variant A/G snv 0.77 0.700 1.000 1 2019 2019
dbSNP: rs6699417
rs6699417
2 1 88657760 intron variant C/T snv 0.61 0.700 1.000 1 2010 2010
dbSNP: rs7551732
rs7551732
1 1 88673358 intron variant T/A snv 0.63 0.700 1.000 1 2014 2014