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: rs13124007
rs13124007
SLC2A9
1 1.000 0.120 4 10042307 intron variant G/A;C snv 0.010 1.000 1 2012 2012
dbSNP: rs10792443
rs10792443
NRXN2
2 0.925 0.120 11 64627780 intron variant G/C snv 0.51 0.700 1.000 3 2010 2013
dbSNP: rs10897526
rs10897526
MAP4K2
2 0.925 0.120 11 64792426 splice region variant T/C snv 0.37 0.30 0.700 1.000 3 2010 2013
dbSNP: rs11231845
rs11231845
NRXN2
2 0.925 0.120 11 64639947 intron variant G/A snv 0.51 0.700 1.000 3 2010 2013
dbSNP: rs12499240
rs12499240
WDR1
2 0.925 0.120 4 10102266 intron variant T/C snv 0.66 0.700 1.000 3 2010 2013
dbSNP: rs13120400
rs13120400
ABCG2
2 0.925 0.120 4 88112375 intron variant T/C snv 0.21 0.700 1.000 3 2010 2013
dbSNP: rs17013584
rs17013584 		2 0.925 0.120 4 87951811 regulatory region variant G/A snv 0.14 0.700 1.000 3 2010 2013
dbSNP: rs2360873
rs2360873
NRXN2
2 0.925 0.120 11 64623685 non coding transcript exon variant G/C snv 0.49 0.700 1.000 3 2010 2013
dbSNP: rs2622604
rs2622604
ABCG2
2 0.925 0.120 4 88157772 intron variant T/A;C snv 0.700 1.000 3 2010 2013
dbSNP: rs2666559
rs2666559
NRXN2
2 0.925 0.120 11 64671755 intron variant G/A;T snv 0.700 1.000 3 2010 2013
dbSNP: rs2725203
rs2725203
PKD2
2 0.925 0.120 4 88074643 intron variant T/A;C snv 0.700 1.000 3 2010 2013
dbSNP: rs2725225
rs2725225
PKD2
2 0.925 0.120 4 88030924 intron variant T/C snv 0.49 0.700 1.000 3 2010 2013
dbSNP: rs2725227
rs2725227
PKD2
2 0.925 0.120 4 88023359 intron variant C/T snv 0.49 0.700 1.000 3 2010 2013
dbSNP: rs2728110
rs2728110
PKD2
2 0.925 0.120 4 88031731 intron variant A/C;G snv 0.700 1.000 3 2010 2013
dbSNP: rs2728119
rs2728119 		2 0.925 0.120 4 87956379 regulatory region variant G/A;C snv 0.700 1.000 3 2010 2013
dbSNP: rs3109823
rs3109823
ABCG2
2 0.925 0.120 4 88143450 intron variant C/T snv 0.65 0.700 1.000 3 2010 2013
dbSNP: rs4393994
rs4393994
WDR1
2 0.925 0.120 4 10113497 intron variant C/G;T snv 0.700 1.000 3 2010 2013
dbSNP: rs492175
rs492175
NRXN2
2 0.925 0.120 11 64665606 intron variant G/A;C snv 0.700 1.000 3 2010 2013
dbSNP: rs500531
rs500531
NRXN2
2 0.925 0.120 11 64719547 intron variant G/T snv 0.50 0.700 1.000 3 2010 2013
dbSNP: rs519090
rs519090
NRXN2
2 0.925 0.120 11 64688768 intron variant G/C snv 0.49 0.700 1.000 3 2010 2013
dbSNP: rs555456
rs555456
NRXN2 ; NRXN2-AS1
2 0.925 0.120 11 64650787 intron variant T/A;C snv 0.700 1.000 3 2010 2013
dbSNP: rs603089
rs603089
SLC17A3
2 0.925 0.120 6 25877742 intron variant G/A snv 0.36 0.700 1.000 3 2010 2013
dbSNP: rs6849736
rs6849736
SLC2A9
2 0.925 0.120 4 9985159 intron variant G/A;C snv 0.700 1.000 3 2010 2013
dbSNP: rs10002984
rs10002984 		2 0.925 0.120 4 9679109 intron variant T/C snv 0.95 0.700 1.000 2 2010 2013
dbSNP: rs10005684
rs10005684 		2 0.925 0.120 4 9625273 intron variant T/A;G snv 0.700 1.000 2 2010 2013