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: rs11207995
rs11207995
DOCK7
4 1 62583880 intron variant A/C;G snv 0.700 1.000 2 2018 2019
dbSNP: rs11220463
rs11220463
ST3GAL4
3 11 126378316 intron variant A/T snv 0.12 0.700 1.000 2 2016 2018
dbSNP: rs112875651
rs112875651 		7 8 125494452 intron variant G/A snv 0.31 0.700 1.000 2 2015 2018
dbSNP: rs114067101
rs114067101 		2 6 32490183 intergenic variant A/G snv 6.1E-05 0.700 1.000 2 2015 2018
dbSNP: rs114197570
rs114197570 		2 19 11085594 upstream gene variant C/T snv 3.3E-03 0.700 1.000 2 2018 2019
dbSNP: rs11621792
rs11621792
NYNRIN
2 14 24402720 intron variant C/T snv 0.32 0.700 1.000 2 2015 2018
dbSNP: rs11648003
rs11648003
DHODH
2 16 72018449 intron variant A/G snv 0.18 0.700 1.000 2 2015 2018
dbSNP: rs1169314
rs1169314
C12orf43
2 12 121005313 intron variant A/C;G snv 0.700 1.000 2 2015 2018
dbSNP: rs117753190
rs117753190
ABCA6
2 17 69140184 intron variant C/G snv 2.0E-02 0.700 1.000 2 2019 2019
dbSNP: rs11784833
rs11784833
GRINA ; PARP10
3 8 143989244 intron variant T/C snv 0.27 0.700 1.000 2 2015 2018
dbSNP: rs11870935
rs11870935
KPNB1
4 17 47655239 intron variant G/A;C snv 0.700 1.000 2 2019 2019
dbSNP: rs12117661
rs12117661 		2 1 55021673 downstream gene variant C/G snv 0.28 0.700 1.000 2 2018 2019
dbSNP: rs12721046
rs12721046
APOC1
8 19 44917997 intron variant G/A snv 0.11 0.700 1.000 2 2012 2012
dbSNP: rs13277801
rs13277801
UBXN2B
2 8 58440975 intron variant C/T snv 0.69 0.700 1.000 2 2017 2018
dbSNP: rs1423527
rs1423527 		2 5 75306874 intergenic variant C/A snv 0.42 0.700 1.000 2 2018 2019
dbSNP: rs143020224
rs143020224
SMARCA4
2 19 11076648 intron variant C/G;T snv 0.700 1.000 2 2018 2019
dbSNP: rs1553318
rs1553318
HAVCR1
3 5 157052312 intron variant G/A;C snv 6.2E-03; 0.67 0.700 1.000 2 2015 2018
dbSNP: rs17242787
rs17242787
LDLR
3 19 11091784 intron variant T/A snv 6.4E-03 0.700 1.000 2 2012 2012
dbSNP: rs17248720
rs17248720
LDLR
4 19 11087511 upstream gene variant C/T snv 0.16 0.700 1.000 2 2012 2012
dbSNP: rs1730859
rs1730859 		2 1 107075085 intergenic variant G/A snv 0.75 0.700 1.000 2 2018 2018
dbSNP: rs174529
rs174529
MYRF ; TMEM258
7 11 61776489 intron variant T/C snv 0.34 0.700 1.000 2 2018 2019
dbSNP: rs174533
rs174533
MYRF ; TMEM258
18 0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 0.700 1.000 2 2017 2019
dbSNP: rs174554
rs174554
FADS1 ; FADS2
7 1.000 0.080 11 61811991 intron variant A/G snv 0.40 0.28 0.700 1.000 2 2018 2019
dbSNP: rs174583
rs174583
FADS2
16 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.700 1.000 2 2018 2019
dbSNP: rs1748195
rs1748195
DOCK7
8 0.851 0.120 1 62583922 intron variant C/G;T snv 0.700 1.000 2 2018 2019