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: rs6535594
rs6535594
NR3C2
2 4 148211605 intron variant G/A snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs10023335
rs10023335
SHROOM3
1 4 76437834 intron variant T/C snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs4665972
rs4665972
SNX17
9 2 27375230 intron variant T/C snv 0.69 0.700 1.000 1 2019 2019
dbSNP: rs147215801
rs147215801
ST8SIA6 ; ST8SIA6-AS1
1 10 17394779 intron variant C/T snv 1.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs16940484
rs16940484
TTC39C
1 18 24102336 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs3784283
rs3784283
TYRO3
1 15 41575584 intron variant A/T snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs78954674
rs78954674
WWC1
1 5 168365677 intron variant G/A snv 3.7E-02 0.700 1.000 1 2018 2018