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: rs4487353
rs4487353 		1 1.000 0.040 4 123332634 intergenic variant G/A snv 0.53 0.700 1.000 1 2018 2018
dbSNP: rs478304
rs478304 		1 1.000 0.040 11 65726789 upstream gene variant G/T snv 0.54 0.700 1.000 1 2014 2014
dbSNP: rs629725
rs629725 		1 1.000 0.040 5 53335237 TF binding site variant T/C snv 0.74 0.700 1.000 1 2018 2018
dbSNP: rs6428829
rs6428829
HSD3B1
2 0.925 0.040 1 119512118 intron variant A/G snv 0.78 0.010 1.000 1 2013 2013
dbSNP: rs6684868
rs6684868 		1 1.000 0.040 1 218674648 TF binding site variant G/A snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs72966077
rs72966077
WNT10A ; LOC105373882
1 1.000 0.040 2 218894507 intron variant C/T snv 3.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs747650
rs747650
C11orf49
1 1.000 0.040 11 47154454 non coding transcript exon variant C/T snv 0.34 0.700 1.000 1 2014 2014
dbSNP: rs7531806
rs7531806
C1orf112 ; LOC107985745
1 1.000 0.040 1 169681903 intron variant G/A snv 0.61 0.700 1.000 1 2014 2014
dbSNP: rs75430906
rs75430906 		1 1.000 0.040 3 20676437 intron variant G/A snv 1.9E-02 0.700 1.000 1 2014 2014
dbSNP: rs7799039
rs7799039
LOC105375494
33 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs7809981
rs7809981
SUGCT
1 1.000 0.040 7 40834777 intron variant G/T snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs788790
rs788790 		1 1.000 0.040 1 202320478 downstream gene variant C/A snv 0.44 0.700 1.000 1 2018 2018