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: rs1042778
rs1042778
CAV3 ; OXTR
3 0.925 0.040 3 8752859 3 prime UTR variant G/A;C;T snv 0.010 1.000 1 2015 2015
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: 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: rs466448
rs466448
APP
4 0.925 0.040 21 26171790 intron variant A/C;G snv 0.010 1.000 1 2013 2013
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 2012 2012
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 2012 2012