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: rs1344706
rs1344706
ZNF804A
21 0.701 0.160 2 184913701 intron variant A/C;T snv 0.010 1.000 1 2019 2019
dbSNP: rs1800544
rs1800544
ADRA2A
12 0.790 0.160 10 111076745 upstream gene variant G/C snv 0.59 0.010 1.000 1 2010 2010
dbSNP: rs3792452
rs3792452
GRM7
2 0.925 0.040 3 7625097 intron variant C/T snv 0.15 0.010 1.000 1 2013 2013
dbSNP: rs6551665
rs6551665
ADGRL3
4 0.882 0.040 4 61873823 intron variant G/A snv 0.59 0.010 1.000 1 2015 2015
dbSNP: rs6782011
rs6782011
GRM7
7 0.807 0.120 3 7457960 intron variant C/T snv 0.52 0.010 1.000 1 2019 2019
dbSNP: rs779867
rs779867
GRM7
9 0.776 0.120 3 7442784 intron variant T/C;G snv 0.010 1.000 1 2019 2019
dbSNP: rs9357271
rs9357271
BTBD9
8 0.776 0.160 6 38398097 intron variant T/C snv 0.38 0.010 1.000 1 2009 2009