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: rs301443
rs301443
SPATA6L
1 1.000 0.040 9 4594919 intron variant C/G snv 0.72 0.050 0.800 5 2010 2019
dbSNP: rs301434
rs301434
SLC1A1 ; SPATA6L
2 0.925 0.040 9 4582082 intron variant C/G;T snv 0.040 1.000 4 2006 2019
dbSNP: rs2228622
rs2228622
SLC1A1 ; SPATA6L
1 1.000 0.040 9 4564432 synonymous variant G/A snv 0.39 0.35 0.030 1.000 3 2007 2019
dbSNP: rs762178
rs762178
OLIG2
2 0.925 0.040 21 33027093 synonymous variant A/G snv 0.51 0.53 0.030 1.000 3 2007 2019
dbSNP: rs10491734
rs10491734 		1 1.000 0.040 9 4482706 intergenic variant T/A;C snv 0.020 1.000 2 2013 2013
dbSNP: rs1059004
rs1059004
OLIG2
4 0.925 0.040 21 33028155 3 prime UTR variant C/A snv 0.41 0.020 1.000 2 2007 2015
dbSNP: rs16965628
rs16965628
SLC6A4
3 0.882 0.040 17 30228407 intron variant G/C snv 0.14 0.020 0.500 2 2015 2018
dbSNP: rs2883187
rs2883187
BDNF
1 1.000 0.040 11 27719545 5 prime UTR variant G/A snv 0.40 0.020 1.000 2 2014 2020
dbSNP: rs3780412
rs3780412
SLC1A1 ; SPATA6L
1 1.000 0.040 9 4572480 intron variant T/C;G snv 0.020 1.000 2 2007 2019
dbSNP: rs6766410
rs6766410
HTR3C
2 1.000 0.040 3 184056974 missense variant C/A;T snv 0.45; 4.0E-06 0.020 1.000 2 2014 2016
dbSNP: rs1000592
rs1000592 		1 1.000 0.040 2 118939624 upstream gene variant C/A snv 6.4E-03 0.010 1.000 1 2014 2014
dbSNP: rs1000952
rs1000952
HTR3D
1 1.000 0.040 3 184038034 missense variant G/A;C;T snv 0.66; 3.6E-05; 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs10042486
rs10042486 		4 0.882 0.040 5 63965502 intron variant C/T snv 0.58 0.010 1.000 1 2019 2019
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: rs11174202
rs11174202
TAFA2
2 0.925 0.040 12 61858476 intron variant A/G snv 0.49 0.700 1.000 1 2018 2018
dbSNP: rs1148374
rs1148374
CDH2
1 1.000 0.040 18 28070318 intron variant T/A snv 0.31 0.010 1.000 1 2016 2016
dbSNP: rs11583978
rs11583978
DLGAP3
2 0.925 0.040 1 34864921 downstream gene variant A/C;G snv 0.010 1.000 1 2011 2011
dbSNP: rs11783752
rs11783752 		2 0.925 0.040 8 20192013 intergenic variant G/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs11854486
rs11854486
TRPM7
1 1.000 0.040 15 50660473 intron variant T/C snv 7.3E-02 0.010 1.000 1 2012 2012
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: rs12536521
rs12536521 		1 1.000 0.040 7 89349373 intergenic variant T/A snv 4.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs12605662
rs12605662
CDH2
1 1.000 0.040 18 28171702 intron variant G/A snv 0.48 0.010 1.000 1 2016 2016
dbSNP: rs12635725
rs12635725 		1 1.000 0.040 3 1895465 intergenic variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1265692223
rs1265692223
HTR3E ; LOC105374249 ; HTR3E-AS1
1 1.000 0.040 3 184100530 missense variant A/G snv 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs12682807
rs12682807
SLC1A1 ; SPATA6L
1 1.000 0.040 9 4574022 splice region variant A/C snv 0.11 8.5E-02 0.010 1.000 1 2013 2013