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: rs1056836
rs1056836
CYP1B1
58 0.581 0.680 2 38071060 missense variant G/C snv 0.51 0.010 1.000 1 2018 2018
dbSNP: rs10809907
rs10809907
MPDZ
3 1.000 9 13134433 non coding transcript exon variant C/G;T snv 0.010 1.000 1 2013 2013
dbSNP: rs1514280
rs1514280
ACE2
3 1.000 X 15568325 intron variant A/G snv 0.010 1.000 1 2013 2013
dbSNP: rs1800440
rs1800440
CYP1B1
29 0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs2104425
rs2104425
LOC105375050
4 0.925 0.040 6 40277470 upstream gene variant T/C snv 0.91 0.010 1.000 1 2017 2017
dbSNP: rs3842803
rs3842803
PTGS1
4 0.925 0.040 9 122392256 synonymous variant T/C snv 2.4E-02 8.2E-02 0.010 1.000 1 2013 2013
dbSNP: rs41423247
rs41423247
NR3C1
23 0.695 0.440 5 143399010 intron variant G/C snv 0.31 0.010 1.000 1 2012 2012
dbSNP: rs466448
rs466448
APP
4 0.925 0.040 21 26171790 intron variant A/C;G snv 0.010 1.000 1 2013 2013
dbSNP: rs53576
rs53576
CAV3 ; OXTR
42 0.641 0.320 3 8762685 intron variant A/G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2019 2019
dbSNP: rs6432860
rs6432860
SCN1A ; SCN1A-AS1
4 0.925 0.080 2 166041354 synonymous variant A/G;T snv 0.73; 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs759834365
rs759834365
BDNF ; BDNF-AS
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.010 1.000 1 2019 2019