Source: CURATED ×
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: rs111365677
rs111365677 		3 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 0.700 1.000 1 2016 2016
dbSNP: rs11209175
rs11209175
GNG12-AS1
2 1.000 0.040 1 67909145 intron variant C/T snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs116362708
rs116362708
SLC44A5
2 1.000 0.040 1 75464629 intron variant G/A snv 2.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs12030991
rs12030991 		2 1.000 0.040 1 106683737 intergenic variant G/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12068879
rs12068879
KAZN
2 1.000 0.040 1 14959860 intron variant A/G snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs12137398
rs12137398
CAMTA1
2 1.000 0.040 1 7730488 intron variant C/T snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs12137936
rs12137936
NEGR1
2 1.000 0.040 1 72254674 intron variant C/G snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs17432675
rs17432675
LMOD1
2 1.000 0.040 1 201918593 intron variant T/C snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs3795310
rs3795310
RERE
2 1.000 0.040 1 8371547 intron variant C/T snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs4554696
rs4554696
PDE4B
2 1 65942328 intron variant C/T snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs4839421
rs4839421
CYMP
3 0.925 0.040 1 110479338 intron variant C/A snv 0.40 0.700 1.000 1 2016 2016
dbSNP: rs6661750
rs6661750
PDE4B
2 1 66081201 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs75507262
rs75507262
LINC02815
2 1.000 0.040 1 229213737 intergenic variant A/G snv 8.0E-03 0.700 1.000 1 2016 2016
dbSNP: rs75650221
rs75650221
RABGAP1L
2 1.000 0.040 1 174452856 intron variant C/T snv 4.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs913687
rs913687
RABGAP1L
2 1.000 0.040 1 174805993 intron variant A/G snv 0.60 0.700 1.000 1 2018 2018
dbSNP: rs113378111
rs113378111 		3 1.000 0.040 2 9788024 intergenic variant G/A snv 2.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs11693031
rs11693031
ERBB4
2 1.000 0.040 2 211813206 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs13413953
rs13413953
ARHGAP15
2 1.000 0.040 2 143479467 intron variant T/G snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs1375194
rs1375194
LOC105374455
2 1.000 0.040 2 33601810 intron variant T/C snv 0.42 0.700 1.000 1 2016 2016
dbSNP: rs16841143
rs16841143
PTH2R
2 2 208384849 intron variant G/A snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs17711053
rs17711053
VWC2L
2 1.000 0.040 2 214574984 intron variant A/G snv 0.11 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: rs190662943
rs190662943
DPP10
2 1.000 0.040 2 115195009 intron variant G/A snv 5.6E-04 0.700 1.000 1 2016 2016
dbSNP: rs2042555
rs2042555 		2 1.000 0.040 2 147797920 intergenic variant G/A snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs2215939
rs2215939
LINC01122
2 1.000 0.040 2 58492312 intron variant T/A snv 0.57 0.700 1.000 1 2018 2018