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: rs1432295
rs1432295
LINC01185
1 1.000 0.120 2 60839531 intron variant G/A snv 0.69 0.800 1.000 2 2010 2013
dbSNP: rs501764
rs501764
GATA3 ; GATA3-AS1
1 1.000 0.120 10 8051071 non coding transcript exon variant G/T snv 0.87 0.86 0.800 1.000 2 2010 2013
dbSNP: rs1002658
rs1002658 		1 1.000 0.120 6 137660447 intron variant C/T snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs1244186
rs1244186
GATA3 ; GATA3-AS1
1 1.000 0.120 10 8050720 non coding transcript exon variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs2069757
rs2069757
TH2LCRR
1 1.000 0.120 5 132662721 intron variant G/A snv 7.5E-02 0.800 1.000 1 2014 2014
dbSNP: rs2240064
rs2240064
CCHCR1
1 1.000 0.120 6 31146796 intron variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs2523710
rs2523710
MICB-DT
1 1.000 0.120 6 31483132 intron variant G/A snv 0.14 0.700 1.000 1 2013 2013
dbSNP: rs2608053
rs2608053
PVT1
1 1.000 0.120 8 128063586 intron variant T/C snv 0.50 0.800 1.000 1 2010 2010
dbSNP: rs2855430
rs2855430
COL11A2
1 1.000 0.120 6 33173503 missense variant G/A snv 0.12 9.9E-02 0.700 1.000 1 2013 2013
dbSNP: rs3093998
rs3093998 		1 1.000 0.120 6 31517397 downstream gene variant C/A snv 0.70 0.700 1.000 1 2013 2013
dbSNP: rs3130237
rs3130237 		1 1.000 0.120 6 33129784 downstream gene variant T/C snv 0.13 0.700 1.000 1 2013 2013
dbSNP: rs4733809
rs4733809
PVT1
1 1.000 0.120 8 127977046 intron variant C/T snv 0.54 0.700 1.000 1 2013 2013
dbSNP: rs485411
rs485411
GATA3 ; GATA3-AS1
1 1.000 0.120 10 8051222 non coding transcript exon variant T/A;C;G snv 0.81 0.700 1.000 1 2013 2013
dbSNP: rs6439924
rs6439924
CLSTN2 ; LOC105374132
1 1.000 0.120 3 140450815 intron variant A/C snv 0.21 0.800 1.000 1 2014 2014
dbSNP: rs6565176
rs6565176 		1 1.000 0.120 16 30163605 intergenic variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs7111520
rs7111520
POU2AF1
1 1.000 0.120 11 111378886 intron variant G/A snv 0.58 0.700 1.000 1 2018 2018
dbSNP: rs752427
rs752427
PVT1
1 1.000 0.120 8 127967762 intron variant C/T snv 0.55 0.700 1.000 1 2013 2013
dbSNP: rs805286
rs805286
LY6G6D ; LY6G6E ; LY6G6F-LY6G6D
1 1.000 0.120 6 31711530 intron variant A/G snv 0.42 0.700 1.000 1 2013 2013
dbSNP: rs9267947
rs9267947 		1 1.000 0.120 6 32243441 intergenic variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs9482849
rs9482849 		1 1.000 0.120 6 127967391 downstream gene variant T/C snv 0.14 0.700 1.000 1 2017 2017
dbSNP: rs387906223
rs387906223
KLHDC8B
1 1.000 0.120 3 49171662 5 prime UTR variant C/T snv 4.8E-03 0.700 0
dbSNP: rs2019960
rs2019960
PVT1
2 0.925 0.160 8 128180025 intron variant T/C snv 0.27 0.800 1.000 3 2010 2014
dbSNP: rs10881578
rs10881578
RXRA
2 0.925 0.240 9 134340689 intron variant A/G snv 0.32 0.010 1.000 1 2018 2018
dbSNP: rs12488654
rs12488654
TNFSF10
2 0.925 0.160 3 172524100 upstream gene variant G/A snv 0.16 0.010 1.000 1 2014 2014
dbSNP: rs13195441
rs13195441 		2 0.925 0.200 6 32775521 intergenic variant G/A snv 0.30 0.700 1.000 1 2013 2013