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: rs12707116
rs12707116
1 7 133740156 intron variant T/C snv 0.48 0.700 1.000 3 2017 2019
dbSNP: rs1362739
rs1362739
2 1.000 0.040 7 133746181 intron variant C/A;T snv 0.48 0.700 1.000 3 2017 2019
dbSNP: rs4728302
rs4728302
1 7 133945710 intron variant C/T snv 0.53 0.700 1.000 3 2017 2019
dbSNP: rs3823572
rs3823572
1 7 133995848 intron variant G/A snv 0.52 0.700 1.000 2 2018 2019
dbSNP: rs6973256
rs6973256
1 7 133370849 intron variant C/T snv 0.64 0.700 1.000 2 2018 2019
dbSNP: rs10215367
rs10215367
1 7 133260999 intron variant C/T snv 0.68 0.700 1.000 1 2019 2019
dbSNP: rs10254118
rs10254118
1 7 133473599 intron variant T/A snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs10281827
rs10281827
1 7 133397056 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1030268
rs1030268
1 7 133921878 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10954428
rs10954428
1 7 133703303 intron variant G/A snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs11765450
rs11765450
1 7 133384928 intron variant C/T snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs11977339
rs11977339
1 7 133285920 intron variant C/T snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs12707087
rs12707087
1 7 133269778 intron variant T/C snv 0.86 0.700 1.000 1 2019 2019
dbSNP: rs12707093
rs12707093
1 7 133516063 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs17167170
rs17167170
1 7 133617591 intron variant A/G snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs17167210
rs17167210
1 7 133654590 intron variant G/A snv 0.41 0.700 1.000 1 2019 2019
dbSNP: rs1882538
rs1882538
1 7 133276984 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2346268
rs2346268
1 7 133957989 intron variant G/A snv 0.69 0.700 1.000 1 2019 2019
dbSNP: rs2346449
rs2346449
1 7 134049164 intron variant G/T snv 0.73 0.700 1.000 1 2018 2018
dbSNP: rs2971963
rs2971963
1 7 133956752 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2971970
rs2971970
1 7 133959025 intron variant T/G snv 0.85 0.700 1.000 1 2019 2019
dbSNP: rs35284403
rs35284403
1 7 133264129 intron variant T/C snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs4422723
rs4422723
1 7 133921405 intron variant A/T snv 0.62 0.700 1.000 1 2019 2019
dbSNP: rs4731992
rs4731992
1 7 134017344 intron variant A/G snv 0.85 0.700 1.000 1 2018 2018
dbSNP: rs6949760
rs6949760
2 7 133991348 intron variant C/A snv 0.73 0.700 1.000 1 2018 2018