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: rs676556
rs676556
BBX
1 3 107648872 intron variant A/G snv 0.23 0.700 1.000 2 2018 2019
dbSNP: rs6861681
rs6861681
CPEB4
1 5 173935455 intron variant G/A snv 0.22 0.800 1.000 2 2010 2018
dbSNP: rs6874524
rs6874524
ARL15
1 5 54047699 intron variant T/C snv 0.31 0.700 1.000 2 2018 2019
dbSNP: rs6908042
rs6908042
CDKAL1
1 6 20589496 intron variant A/G snv 0.27 0.700 1.000 2 2018 2019
dbSNP: rs6920788
rs6920788
TRMT11
1 6 126010842 intron variant C/A;T snv 0.700 1.000 2 2018 2019
dbSNP: rs7020604
rs7020604
PALM2AKAP2
1 9 109821274 intron variant A/G snv 0.33 0.700 1.000 2 2019 2019
dbSNP: rs710122
rs710122
TBC1D22A
1 22 46802158 intron variant G/A snv 0.69 0.700 1.000 2 2018 2019
dbSNP: rs711869
rs711869 		1 2 12933841 intron variant G/A;C snv 0.700 1.000 2 2018 2019
dbSNP: rs7133378
rs7133378
CCDC92 ; DNAH10
6 12 123924955 intron variant G/A snv 0.38 0.700 1.000 2 2018 2019
dbSNP: rs718314
rs718314
LOC105369705
6 0.882 0.120 12 26300350 intron variant A/G snv 0.27 0.800 1.000 2 2010 2018
dbSNP: rs747249
rs747249
ZBTB44-DT
1 11 130401752 intron variant A/G;T snv 0.71 0.700 1.000 2 2018 2019
dbSNP: rs7492628
rs7492628
DGLUCY
1 14 91080792 intron variant C/G snv 0.38 0.700 1.000 2 2018 2019
dbSNP: rs7801581
rs7801581
HOXA11 ; HOXA11-AS
5 7 27184152 intron variant C/T snv 0.24 0.700 1.000 2 2015 2018
dbSNP: rs780159
rs780159
ZMIZ1
2 10 79147390 intron variant A/C;G snv 0.700 1.000 2 2018 2019
dbSNP: rs7932891
rs7932891
ZBED5-AS1
1 11 10899965 intron variant A/G snv 0.73 0.700 1.000 2 2019 2019
dbSNP: rs797486
rs797486
DLEU1 ; DLEU7
2 13 50647482 intron variant C/A snv 0.85 0.700 1.000 2 2018 2019
dbSNP: rs863750
rs863750
RFLNA ; ZNF664-RFLNA
7 12 124020897 intron variant C/T snv 0.53 0.700 1.000 2 2015 2019
dbSNP: rs910382
rs910382
TSHZ2
1 20 53082650 intron variant G/A snv 0.43 0.700 1.000 2 2018 2019
dbSNP: rs929641
rs929641
LINC01122
3 2 58565242 intron variant A/G snv 0.45 0.700 1.000 2 2015 2019
dbSNP: rs9491696
rs9491696
RSPO3
2 6 127131494 intron variant C/G snv 0.45 0.800 1.000 2 2010 2015
dbSNP: rs9644033
rs9644033
LOC107986930
1 8 23753126 intron variant A/T snv 0.25 0.700 1.000 2 2018 2019
dbSNP: rs9647379
rs9647379
FNDC3B
2 3 172067378 intron variant G/C snv 0.32 0.700 1.000 2 2018 2019
dbSNP: rs9837325
rs9837325
PLXND1
1 3 129596988 intron variant C/A snv 0.22 0.700 1.000 2 2018 2019
dbSNP: rs984222
rs984222
TBX15
3 1 118961220 intron variant C/A;G snv 0.800 1.000 2 2010 2019
dbSNP: rs998749
rs998749
MECOM
1 3 169255014 intron variant A/G snv 0.40 0.700 1.000 2 2018 2019