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: rs2295193
rs2295193
SYNE1
1 1.000 0.040 6 152131959 intron variant G/A;C snv 0.030 0.667 3 2010 2014
dbSNP: rs11174202
rs11174202
TAFA2
2 0.925 0.040 12 61858476 intron variant A/G snv 0.49 0.700 1.000 2 2017 2018
dbSNP: rs726281
rs726281
ESR1
1 1.000 0.040 6 151981443 intron variant G/A snv 0.56 0.020 1.000 2 2010 2014
dbSNP: rs10070190
rs10070190 		2 0.925 0.040 5 26866262 intergenic variant G/A snv 0.60 0.010 1.000 1 2013 2013
dbSNP: rs10096097
rs10096097
DCTN6 ; LEPROTL1
1 1.000 0.040 8 30169582 intron variant G/A snv 0.62 0.010 1.000 1 2011 2011
dbSNP: rs10747478
rs10747478 		1 1.000 0.040 1 96435899 intergenic variant T/A;C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs11179027
rs11179027
TPH2
1 1.000 0.040 12 71983532 intron variant G/C snv 0.26 0.010 1.000 1 2013 2013
dbSNP: rs11783752
rs11783752 		2 0.925 0.040 8 20192013 intergenic variant G/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs117957029
rs117957029
LOC105370064
1 1.000 0.040 12 127200688 intron variant T/C snv 1.4E-02 0.700 1.000 1 2017 2017
dbSNP: rs12504244
rs12504244 		2 0.925 0.040 4 54619021 intergenic variant C/A;G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1285957
rs1285957 		1 1.000 0.040 7 141889478 downstream gene variant T/C snv 0.86 0.700 1.000 1 2013 2013
dbSNP: rs1298806501
rs1298806501
ESR2
1 1.000 0.040 14 64227600 missense variant G/A snv 4.0E-06 0.010 1.000 1 1998 1998
dbSNP: rs13100344
rs13100344 		1 1.000 0.040 3 94886263 intergenic variant T/A snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs13125782
rs13125782
SORCS2
1 1.000 0.040 4 7426539 intron variant T/A;C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs13338499
rs13338499
LOC101927837
2 0.925 0.040 16 67486220 intron variant A/G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs1356639869
rs1356639869
NPY ; LOC107986777
2 1.000 0.040 7 24289527 missense variant C/A snv 0.010 1.000 1 2007 2007
dbSNP: rs145241704
rs145241704 		1 1.000 0.040 7 141805287 upstream gene variant T/G snv 7.4E-02 0.800 1.000 1 2013 2013
dbSNP: rs200312312
rs200312312
LOC105379109
1 1.000 0.040 5 104666645 intron variant T/C snv 0.16 0.700 1.000 1 2017 2017
dbSNP: rs2008387
rs2008387
MGMT
1 1.000 0.040 10 129650500 intron variant G/A snv 0.36 0.700 1.000 1 2019 2019
dbSNP: rs2287348
rs2287348
ERLEC1 ; ASB3 ; GPR75-ASB3
1 1.000 0.040 2 53812676 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2834070
rs2834070 		2 0.925 0.040 21 33015144 intron variant G/T snv 0.24 0.010 1.000 1 2013 2013
dbSNP: rs370838138
rs370838138 		1 1.000 0.040 5 25081736 intergenic variant G/C snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs3749073
rs3749073
GPR55
1 1.000 0.040 2 230910379 missense variant C/A snv 0.12 0.17 0.010 1.000 1 2011 2011
dbSNP: rs3825885
rs3825885
NTRK3
1 1.000 0.040 15 88059610 intron variant T/C snv 0.32 0.010 1.000 1 2013 2013
dbSNP: rs4825476
rs4825476
GRIA3
2 0.925 0.040 X 123307628 intron variant G/A;C snv 0.010 1.000 1 2013 2013