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: rs2576391
rs2576391
ABI3BP
1 3 100958166 intron variant C/G snv 0.86 0.700 1.000 1 2010 2010
dbSNP: rs2595893
rs2595893
ABI3BP
1 3 100958998 intron variant C/T snv 0.86 0.700 1.000 1 2010 2010
dbSNP: rs2595894
rs2595894
ABI3BP
1 3 100959038 intron variant G/A;C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs2602098
rs2602098
SLC4A4
1 4 71269738 intron variant T/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs2713782
rs2713782
ABI3BP
1 3 100910460 intron variant G/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs2713787
rs2713787
ABI3BP
1 3 100905594 intron variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs2713793
rs2713793
ABI3BP
1 3 100900330 intron variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs4060963
rs4060963
ABI3BP
1 3 100905717 intron variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs4928096
rs4928096
ABI3BP
1 3 100900916 intron variant G/A snv 0.85 0.700 1.000 1 2010 2010
dbSNP: rs7431835
rs7431835
ABI3BP
1 3 100923879 intron variant T/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs9832195
rs9832195
ABI3BP
1 3 100903548 intron variant A/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs10170138
rs10170138
LRRTM4
1 2 76794802 intron variant C/T snv 0.16 0.700 1.000 1 2012 2012
dbSNP: rs1517782
rs1517782
LRRTM4
1 2 76794100 intron variant C/A snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs2150127
rs2150127
GPC6 ; GPC6-AS2
1 13 93838807 intron variant A/G snv 7.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs300774
rs300774 		3 0.925 0.040 2 112496 intergenic variant A/C;T snv 0.800 1.000 1 2012 2012
dbSNP: rs7296262
rs7296262
TMEM132C
2 1.000 0.040 12 128610527 intron variant T/C;G snv 0.800 1.000 1 2012 2012
dbSNP: rs17173608
rs17173608
RARRES2
8 0.807 0.240 7 150339575 intron variant T/G snv 0.11 0.700 1.000 1 2014 2014
dbSNP: rs17387100
rs17387100
PROM1
3 0.925 0.040 4 15993502 intron variant A/G snv 7.5E-02 0.700 1.000 1 2014 2014
dbSNP: rs112504494
rs112504494
KCNMB2 ; KCNMB2-AS1
1 3 178689358 intron variant G/A snv 7.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs112595860
rs112595860
FGD4
1 12 32487657 intron variant C/G snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs11762112
rs11762112 		1 7 27486673 intergenic variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs150801052
rs150801052
RBFOX2
1 22 35859882 intron variant T/- delins 1.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs16841143
rs16841143
PTH2R
2 2 208384849 intron variant G/A snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs182087934
rs182087934 		2 2 183742707 intergenic variant G/A snv 0.700 1.000 1 2018 2018
dbSNP: rs384005
rs384005
MEF2C-AS2
2 5 88709286 intron variant T/C snv 0.70 0.700 1.000 1 2018 2018