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: rs10110651
rs10110651 		1 8 36989597 upstream gene variant T/C;G snv 0.700 1.000 2 2016 2018
dbSNP: rs17625845
rs17625845 		1 2 120332155 intergenic variant T/C snv 0.15 0.800 1.000 2 2012 2016
dbSNP: rs9397437
rs9397437 		2 1.000 0.080 6 151631197 intergenic variant G/A snv 6.6E-02 0.700 1.000 2 2016 2018
dbSNP: rs10096213
rs10096213 		1 8 36995695 regulatory region variant C/T snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs12173570
rs12173570 		1 6 151636579 intergenic variant C/T snv 0.21 0.800 1.000 1 2012 2012
dbSNP: rs12371778
rs12371778 		1 12 28003148 intergenic variant C/A;G snv 0.800 1.000 1 2012 2012
dbSNP: rs146992477
rs146992477 		1 8 36984537 downstream gene variant -/CTTTCTTTCT delins 0.25 0.700 1.000 1 2018 2018
dbSNP: rs1838564
rs1838564 		1 12 28001962 intergenic variant G/A snv 8.1E-02 0.700 1.000 1 2016 2016
dbSNP: rs2359714
rs2359714 		1 1 118227648 intergenic variant C/T snv 0.44 0.700 1.000 1 2016 2016
dbSNP: rs4820792
rs4820792 		1 22 28765019 intergenic variant C/T snv 0.21 0.800 1.000 1 2012 2012
dbSNP: rs4849887
rs4849887 		7 0.807 0.080 2 120487546 intergenic variant T/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs5752793
rs5752793 		1 22 28764326 intergenic variant A/G snv 0.35 0.700 1.000 1 2016 2016
dbSNP: rs61280460
rs61280460 		1 14 94329847 intergenic variant A/C;T snv 0.800 1.000 1 2012 2012
dbSNP: rs62105303
rs62105303 		1 2 632922 intergenic variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs6427508
rs6427508 		1 1 160269067 intron variant T/C snv 0.63 0.700 1.000 1 2016 2016
dbSNP: rs6557160
rs6557160 		2 6 151628447 intergenic variant A/C snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs7659874
rs7659874 		1 4 74621799 regulatory region variant A/G snv 0.32 0.700 1.000 1 2016 2016
dbSNP: rs7816345
rs7816345 		1 8 36988591 upstream gene variant C/T snv 0.26 0.800 1.000 1 2012 2012
dbSNP: rs17001868
rs17001868
ADSL ; SGSM3 ; LOC107985538
3 0.925 0.080 22 40382227 intron variant A/C snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs11446767
rs11446767
ESR1
1 6 151754327 intron variant TT/-;T;TTT;TTTT;TTTTT;TTTTTTTT;TTTTTTTTTT;TTTTTTTTTTTTTTTTT delins 0.700 1.000 1 2018 2018
dbSNP: rs3205718
rs3205718
FAIM2
2 12 49868026 3 prime UTR variant C/T snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs62033406
rs62033406
FTO
5 16 53790314 intron variant A/G snv 0.33 0.700 1.000 1 2016 2016
dbSNP: rs34091558
rs34091558
LMOD1
2 1.000 0.040 1 201917642 intron variant A/- delins 0.25 0.700 1.000 1 2016 2016
dbSNP: rs62314947
rs62314947
LOC107986229
1 4 74577305 intron variant C/T snv 0.30 0.800 1.000 1 2012 2012
dbSNP: rs200550907
rs200550907
MARK1
1 1 220527823 upstream gene variant -/AAAA delins 0.700 1.000 1 2016 2016