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: rs10011838
rs10011838 		3 1.000 0.080 4 152599127 intergenic variant G/A snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs10039206
rs10039206 		2 5 56692951 intergenic variant T/C snv 0.61 0.700 1.000 1 2019 2019
dbSNP: rs10049088
rs10049088
LINC02029
3 3 157079859 upstream gene variant C/T snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs10065892
rs10065892
AP3B1
2 5 78267439 intron variant G/A snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs10071838
rs10071838
LMBRD2 ; MIR580
2 5 36147704 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10099100
rs10099100 		3 8 10719265 downstream gene variant G/C snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs10132033
rs10132033
PPP1R36
2 14 64556852 intron variant T/C snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs10132060
rs10132060
SLC7A8
2 14 23128526 intron variant C/T snv 0.13 0.700 1.000 1 2019 2019
dbSNP: rs10159676
rs10159676 		2 10 50302023 downstream gene variant G/A snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs10194817
rs10194817
FKBP1B ; WDCP ; MFSD2B
2 2 24034181 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10223451
rs10223451 		2 6 139630553 intron variant A/G snv 0.58 0.700 1.000 1 2016 2016
dbSNP: rs10224902
rs10224902
ANLN
2 7 36415868 synonymous variant T/C snv 0.13 0.12 0.700 1.000 1 2019 2019
dbSNP: rs10254125
rs10254125
EIF2AK1
2 7 6027315 intron variant A/G snv 0.65 0.700 1.000 1 2019 2019
dbSNP: rs10263707
rs10263707
PRKAG2
2 7 151706419 intron variant T/G snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs1029555
rs1029555 		2 7 26547477 upstream gene variant T/C snv 0.80 0.700 1.000 1 2019 2019
dbSNP: rs10410723
rs10410723
RAB8A
2 19 16124498 non coding transcript exon variant C/A snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs10410869
rs10410869 		2 19 57629913 upstream gene variant G/T snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs10414846
rs10414846
HAMP
3 19 35281568 intron variant C/T snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs1042034
rs1042034
APOB
15 0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 0.700 1.000 1 2019 2019
dbSNP: rs10424080
rs10424080 		2 19 18407968 TF binding site variant C/T snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs10424619
rs10424619
USF2
2 19 35277334 non coding transcript exon variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1043897
rs1043897
GALNT2
2 1 230280653 3 prime UTR variant G/T snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs10448
rs10448
CENPBD1P1
2 19 58581872 non coding transcript exon variant T/C snv 0.53 0.700 1.000 1 2019 2019
dbSNP: rs10479001
rs10479001
PDLIM4 ; P4HA2
2 5 132272028 missense variant C/T snv 4.6E-02 7.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs1047912
rs1047912
DIP2B
3 12 50745079 3 prime UTR variant C/T snv 0.21 0.700 1.000 1 2019 2019