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: rs150900094
rs150900094 		1 15 87284961 intergenic variant A/C snv 2.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs61751117
rs61751117
RAB11A ; DENND4A
1 15 65741731 synonymous variant A/C snv 2.6E-02 2.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs73705514
rs73705514
ZNF804B
1 7 88777238 intron variant A/C snv 8.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs705119
rs705119
GC
1 4 71747319 intron variant A/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs9679781
rs9679781
CTNNBL1
1 20 37843596 intron variant A/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs12268753
rs12268753
PRKG1
1 10 52058389 intron variant A/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs7557162
rs7557162 		1 2 177057129 intron variant A/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs111882035
rs111882035
ARHGAP24
1 4 85495401 intron variant A/G snv 1.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs117609474
rs117609474
LINC02331
1 14 53804550 intron variant A/G snv 1.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs118130881
rs118130881
LOC101929492
1 8 31371254 intron variant A/G snv 0.700 1.000 1 2018 2018
dbSNP: rs16873450
rs16873450
STK31
1 7 23767021 intron variant A/G snv 0.55 0.700 1.000 1 2017 2017
dbSNP: rs16986890
rs16986890
CTNNBL1
1 20 37698121 intron variant A/G snv 9.3E-02 0.700 1.000 1 2013 2013
dbSNP: rs2976464
rs2976464
ZNF250
2 1.000 0.040 8 144902955 upstream gene variant A/G snv 0.46 0.700 1.000 1 2018 2018
dbSNP: rs4420638
rs4420638
APOC1
43 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.700 1.000 1 2015 2015
dbSNP: rs9528384
rs9528384 		1 13 61728432 regulatory region variant A/G snv 0.23 0.700 1.000 1 2015 2015
dbSNP: rs145471199
rs145471199 		1 7 9407441 intergenic variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs4776997
rs4776997 		1 15 67858585 intron variant A/G;T snv 0.77 0.700 1.000 1 2015 2015
dbSNP: rs147828834
rs147828834
FSIP1
1 15 39602982 intron variant A/T snv 8.3E-03 0.700 1.000 1 2018 2018
dbSNP: rs139139710
rs139139710
GALNT17
1 7 71678504 intron variant C/A snv 2.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs3801203
rs3801203
GLI3
1 7 42148801 intron variant C/A snv 0.13 0.700 1.000 1 2017 2017
dbSNP: rs112108866
rs112108866
CAPN12
1 19 38761240 intron variant C/A;G snv 1.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs4942792
rs4942792
PDS5B
1 13 32663326 intron variant C/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs113338984
rs113338984
SNTB2
1 16 69282015 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs117905930
rs117905930 		2 1.000 0.080 9 88973603 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs147906088
rs147906088 		2 1.000 0.080 7 54496119 intergenic variant C/A;T snv 0.700 1.000 1 2018 2018