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: rs12566985
rs12566985
2 1 74536509 intron variant G/A snv 0.42 0.700 1.000 4 2015 2017
dbSNP: rs1514175
rs1514175
4 1.000 0.080 1 74525960 intron variant A/G snv 0.48 0.700 1.000 2 2010 2013
dbSNP: rs12041852
rs12041852
1 1 74537816 intron variant G/A snv 0.41 0.700 1.000 1 2016 2016
dbSNP: rs12042908
rs12042908
1 1 74532078 intron variant A/G snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs1514174
rs1514174
2 1.000 0.080 1 74527379 intron variant C/T snv 0.44 0.700 1.000 1 2015 2015
dbSNP: rs1514177
rs1514177
2 1.000 0.080 1 74525718 intron variant C/G snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs7526762
rs7526762
2 1 74527634 intron variant A/G snv 0.42 0.700 1.000 1 2017 2017
dbSNP: rs7551507
rs7551507
2 1 74529541 intron variant C/T snv 0.41 0.700 1.000 1 2017 2017
dbSNP: rs7553158
rs7553158
1 1 74539554 intron variant G/A snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs7553348
rs7553348
2 1 74539383 intron variant G/A snv 0.42 0.700 1.000 1 2015 2015
dbSNP: rs953567
rs953567
1 1 74511741 intron variant A/G snv 0.42 0.700 1.000 1 2019 2019