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: rs10202630
rs10202630 		4 0.882 2 190398199 intergenic variant T/C snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs1020388
rs1020388 		2 5 56264200 upstream gene variant T/G snv 0.34 0.800 1.000 1 2011 2011
dbSNP: rs10444776
rs10444776
LOC112268138
4 0.882 14 105647030 upstream gene variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10460003
rs10460003
LINC01882
2 18 12747013 intron variant C/T snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs10494079
rs10494079
VAV3
4 0.882 1 107832253 intron variant G/C snv 9.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs1052237
rs1052237
NUS1
1 6 117694118 stop gained T/C;G snv 8.8E-05 8.4E-05 0.010 1.000 1 2013 2013
dbSNP: rs10752747
rs10752747
MMEL1
2 1 2593476 intron variant G/T snv 0.41 0.700 1.000 1 2011 2011
dbSNP: rs10892286
rs10892286
DDX6
2 11 118771376 intron variant A/C snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs10932019
rs10932019 		2 2 203764087 downstream gene variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs10937560
rs10937560
MB21D2
4 0.882 3 192909627 intron variant G/C snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs10986284
rs10986284 		4 0.882 9 124236874 intergenic variant A/T snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs11043097
rs11043097
LINC02752
2 11 11114248 intron variant T/C snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs11086102
rs11086102 		6 0.882 19 18287818 upstream gene variant G/C snv 0.64 0.700 1.000 1 2019 2019
dbSNP: rs11571319
rs11571319
CTLA4
1 2 203874215 downstream gene variant G/A snv 0.17 0.010 1.000 1 2012 2012
dbSNP: rs11746555
rs11746555
SLC22A5
4 0.882 5 132391341 intron variant G/A snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs11785816
rs11785816
LINC00824
4 0.882 8 128518940 intron variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs1194849
rs1194849
SPRED2
2 2 65379519 intron variant T/C snv 0.49 0.700 1.000 1 2011 2011
dbSNP: rs11984075
rs11984075
ELMO1
2 7 37397251 intron variant A/G snv 0.14 0.800 1.000 1 2011 2011
dbSNP: rs1199047
rs1199047
CCDC88B
4 0.882 11 64350711 intron variant A/C snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs12138909
rs12138909
MMEL1
2 1 2607299 intron variant C/T snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs12980063
rs12980063
CPT1C
4 0.882 19 49693735 intron variant A/G snv 0.48 0.700 1.000 1 2019 2019
dbSNP: rs1320344
rs1320344
C12orf42
4 0.882 12 103493699 intron variant A/G snv 0.64 0.700 1.000 1 2019 2019
dbSNP: rs13299616
rs13299616
PSMD5 ; CUTALP
4 0.882 9 120832525 intron variant T/C snv 0.50 0.700 1.000 1 2019 2019
dbSNP: rs1331108652
rs1331108652
PIK3CB
1 3 138694820 stop gained G/A snv 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs1333739
rs1333739
RAVER2
1 1 64827766 intron variant A/G;T snv 0.62 0.010 1.000 1 2012 2012