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: rs72675531
rs72675531
LOC105378741
1 1 56111740 intergenic variant A/C snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs75859969
rs75859969 		1 16 50126826 intron variant A/C snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs76721774
rs76721774
CUX2
1 12 111268872 intron variant A/C snv 1.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs77696237
rs77696237
CDH12
1 5 22076380 intron variant A/C snv 1.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs77940566
rs77940566 		2 6 42542864 intergenic variant A/C snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs78784853
rs78784853
TXNDC11
1 16 11723610 intron variant A/C snv 6.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs8085287
rs8085287
RBBP8
1 18 22884208 intron variant A/C snv 0.68 0.700 1.000 1 2019 2019
dbSNP: rs874844
rs874844
KIRREL1
1 1 158097257 3 prime UTR variant A/C snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs9858874
rs9858874
LSAMP
1 3 116782013 intron variant A/C snv 7.8E-03 0.700 1.000 1 2011 2011
dbSNP: rs112389236
rs112389236
LAMA3
1 18 23903604 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs112505971
rs112505971
ANKRD26
13 10 27068541 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs1512282
rs1512282
LOC105377462
5 4 144510345 intron variant A/C;G snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs2865805
rs2865805
AUTS2
1 7 69853209 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs311629
rs311629
S1PR4
1 19 3180805 upstream gene variant A/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs34089598
rs34089598
KLF3
1 4 38675606 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs3820677
rs3820677
KIRREL1
1 1 158098554 3 prime UTR variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs6588216
rs6588216
SGIP1
1 1 66680164 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs67584485
rs67584485
THADA
1 2 43535056 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs6831368
rs6831368
TBC1D14
1 4 6968192 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs8017228
rs8017228
STXBP6
2 14 24980020 intron variant A/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs9869574
rs9869574
BBX
1 3 107662804 5 prime UTR variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10848737
rs10848737
TULP3
1 12 2911478 intron variant A/C;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11039436
rs11039436 		2 11 47866484 intergenic variant A/C;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11264845
rs11264845 		1 1 157901307 upstream gene variant A/C;G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs12034864
rs12034864 		2 1 159215190 regulatory region variant A/C;G;T snv 0.700 1.000 1 2011 2011