Gene: WDR72 ×
Source: ALL
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: rs1031755
rs1031755
WDR72
1 15 53659238 intron variant A/C snv 0.22 0.700 1.000 1 2016 2016
dbSNP: rs10518732
rs10518732
WDR72
2 15 53646845 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10851543
rs10851543
WDR72
1 15 53670551 intron variant A/G snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs17730281
rs17730281
WDR72
3 1.000 0.080 15 53615751 missense variant G/A snv 0.26 0.22 0.700 1.000 1 2019 2019
dbSNP: rs1906436
rs1906436
WDR72
3 1.000 0.040 15 53590245 intron variant T/C snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs35255404
rs35255404
WDR72
1 15 53627029 intron variant G/A snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs35258188
rs35258188
WDR72
4 1.000 0.040 15 53705141 missense variant T/G snv 3.5E-03 1.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs491567
rs491567
WDR72
4 1.000 0.080 15 53654396 intron variant A/C snv 0.34 0.700 1.000 1 2016 2016
dbSNP: rs5812700
rs5812700
WDR72
1 15 53629192 intron variant AGAGAG/-;AG;AGAG;AGAGAGAG;AGAGAGAGAG;AGAGAGAGAGAG;AGAGAGAGAGAGAG delins 0.700 1.000 1 2019 2019
dbSNP: rs62005941
rs62005941
WDR72
1 15 53623569 intron variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs690428
rs690428
WDR72
1 15 53658381 intron variant A/C snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs7169329
rs7169329
WDR72
1 15 53610429 intron variant C/G snv 0.62 0.700 1.000 1 2019 2019