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: rs10795656
rs10795656 		4 1.000 0.080 10 8553876 intergenic variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10852622
rs10852622
ZFPM1
2 16 88490472 intron variant A/G snv 0.35 0.700 1.000 1 2016 2016
dbSNP: rs10858740
rs10858740 		5 12 88451258 intergenic variant A/G;T snv 0.56 0.700 1.000 1 2016 2016
dbSNP: rs10893844
rs10893844 		2 11 128315955 regulatory region variant G/C snv 0.36 0.700 1.000 1 2016 2016
dbSNP: rs10995240
rs10995240
ZNF365 ; LOC105378327
2 10 62628871 intron variant G/C snv 0.29 0.700 1.000 1 2016 2016
dbSNP: rs11065979
rs11065979 		12 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs11127153
rs11127153
PLB1
2 2 28463094 intron variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs11137087
rs11137087 		2 8 7048518 intergenic variant A/G snv 0.60 0.700 1.000 1 2016 2016
dbSNP: rs111759324
rs111759324 		2 1 101186966 upstream gene variant C/T snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs111930700
rs111930700
ACVR1B
4 12 51967869 intron variant C/G snv 8.4E-02 0.700 1.000 1 2016 2016
dbSNP: rs11204682
rs11204682
ENSA
4 1 150623061 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs112401631
rs112401631 		8 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 0.700 1.000 1 2016 2016
dbSNP: rs112505971
rs112505971
ANKRD26
13 10 27068541 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs11319879
rs11319879
HHEX
2 10 92693719 intron variant A/- delins 0.53 0.700 1.000 1 2016 2016
dbSNP: rs11327184
rs11327184
CCDC26
4 8 129592027 intron variant C/- delins 0.40 0.700 1.000 1 2016 2016
dbSNP: rs113422568
rs113422568
SUFU
2 10 102578181 intron variant G/A snv 0.25 0.700 1.000 1 2016 2016
dbSNP: rs113473633
rs113473633
NFKB1
4 1.000 0.040 4 102527974 intron variant A/G snv 1.6E-02 0.700 1.000 1 2016 2016
dbSNP: rs11353326
rs11353326
ARIH2
2 3 48941172 intron variant AAAAA/-;A;AA;AAA;AAAA;AAAAAA;AAAAAAA delins 0.700 1.000 1 2016 2016
dbSNP: rs11359909
rs11359909 		4 3 128603031 intergenic variant G/- delins 0.89 0.700 1.000 1 2016 2016
dbSNP: rs113604586
rs113604586
ALOX15
2 17 4639054 missense variant T/C snv 1.7E-03 1.6E-03 0.700 1.000 1 2016 2016
dbSNP: rs11361923
rs11361923
NOXRED1
4 14 77396337 intron variant C/- delins 0.54 0.700 1.000 1 2016 2016
dbSNP: rs113721499
rs113721499 		1 6 31261530 intergenic variant C/T snv 0.700 1.000 1 2018 2018
dbSNP: rs114050631
rs114050631 		5 2 218156235 regulatory region variant C/T snv 6.9E-03 0.700 1.000 1 2016 2016
dbSNP: rs114269697
rs114269697
JAK1
3 1.000 0.040 1 64848529 intron variant C/A snv 7.3E-03 0.700 1.000 1 2016 2016
dbSNP: rs11428934
rs11428934
CA11 ; SEC1P
4 19 48640988 intron variant -/G ins 0.700 1.000 1 2016 2016