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: rs77924615
rs77924615
PDILT
7 1.000 0.080 16 20381010 intron variant G/A snv 0.16 0.700 1.000 7 2016 2019
dbSNP: rs881858
rs881858
LOC105375069 ; LOC107986598
7 0.882 0.200 6 43838872 intron variant G/A;C snv 0.700 1.000 6 2016 2019
dbSNP: rs2279463
rs2279463
SLC22A2
4 1.000 0.080 6 160247357 intron variant A/G;T snv 0.700 1.000 5 2016 2019
dbSNP: rs80282103
rs80282103
LARP4B
4 1.000 0.080 10 853131 intron variant A/T snv 0.12 0.700 1.000 5 2017 2019
dbSNP: rs8096658
rs8096658
NFATC1 ; LOC107985163
5 0.925 0.120 18 79396537 intron variant C/G snv 0.39 0.700 1.000 5 2016 2019
dbSNP: rs1275609
rs1275609
LOC105369844
3 12 75877403 intron variant G/A snv 0.40 0.700 1.000 4 2018 2019
dbSNP: rs16942751
rs16942751
AQP4-AS1
3 1.000 0.080 18 26813249 intron variant C/A;T snv 0.700 1.000 4 2018 2019
dbSNP: rs2039424
rs2039424
PIP5K1B
2 1.000 0.080 9 68817258 intron variant G/A snv 0.63 0.700 1.000 4 2019 2019
dbSNP: rs3812036
rs3812036
SLC34A1
5 0.925 0.120 5 177386403 intron variant C/T snv 0.23 0.20 0.700 1.000 4 2017 2019
dbSNP: rs10265221
rs10265221
PRKAG2
3 7 151717243 intron variant T/A;C snv 0.700 1.000 3 2016 2019
dbSNP: rs10994856
rs10994856
A1CF
5 0.925 0.120 10 50885488 intron variant G/A snv 0.19 0.700 1.000 3 2017 2019
dbSNP: rs13146355
rs13146355
SHROOM3
6 1.000 0.040 4 76490987 intron variant G/A snv 0.33 0.700 1.000 3 2017 2019
dbSNP: rs1719934
rs1719934
EPB41L3
1 18 5585159 intron variant A/G snv 0.37 0.700 1.000 3 2019 2019
dbSNP: rs187355703
rs187355703
HOXD8 ; LOC100129455 ; HOXD-AS2
4 1.000 0.080 2 176128855 intron variant C/G snv 1.5E-02 1.5E-02 0.700 1.000 3 2017 2019
dbSNP: rs2273684
rs2273684
GSS
2 1.000 0.040 20 34941963 intron variant T/G snv 0.52 0.700 1.000 3 2019 2019
dbSNP: rs2337106
rs2337106
SMAD7
4 18 48934533 intron variant C/A;G snv 0.700 1.000 3 2018 2019
dbSNP: rs2823139
rs2823139 		5 1.000 0.080 21 15204463 intron variant G/A snv 0.34 0.700 1.000 3 2019 2019
dbSNP: rs4744712
rs4744712
PIP5K1B
4 1.000 0.080 9 68819791 intron variant A/C;T snv 0.700 1.000 3 2016 2019
dbSNP: rs7475348
rs7475348
MYPN
2 10 68205420 intron variant C/T snv 0.41 0.700 1.000 3 2018 2019
dbSNP: rs780093
rs780093
GCKR
30 0.763 0.240 2 27519736 intron variant T/C snv 0.68 0.700 1.000 3 2017 2019
dbSNP: rs10224002
rs10224002
PRKAG2
12 0.925 0.080 7 151717955 intron variant A/G snv 0.31 0.700 1.000 2 2018 2019
dbSNP: rs10254101
rs10254101
PRKAG2
3 7 151718450 intron variant C/T snv 0.23 0.700 1.000 2 2017 2019
dbSNP: rs10746942
rs10746942
PIP5K1B
2 9 68819549 intron variant G/A snv 0.63 0.700 1.000 2 2017 2019
dbSNP: rs10774020
rs10774020
SLC6A13
1 12 239710 intron variant T/C snv 0.58 0.700 1.000 2 2019 2019
dbSNP: rs10823156
rs10823156
MYPN
1 10 68192084 intron variant G/C snv 0.45 0.700 1.000 2 2019 2019