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: rs10766471
rs10766471
GTF2H1
1 11 18345583 intron variant C/T snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs10772280
rs10772280
KLRC2
2 12 10428441 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10786774
rs10786774
STN1
1 10 103884565 intron variant G/C snv 0.90 0.700 1.000 1 2019 2019
dbSNP: rs1078859
rs1078859
LYST
1 1 235748725 intron variant C/A snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs10793565
rs10793565
TMEM72-AS1
3 10 44892783 intron variant G/C snv 0.53 0.700 1.000 1 2019 2019
dbSNP: rs10801682
rs10801682
PKN2
1 1 88708570 intron variant A/T snv 0.50 0.700 1.000 1 2019 2019
dbSNP: rs10833106
rs10833106
NAV2
1 11 19401081 intron variant A/G snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs10846742
rs10846742
SCARB1
2 12 124824136 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10849020
rs10849020 		3 12 4222843 intergenic variant C/G snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs1085244
rs1085244
PIK3R3 ; P3R3URF-PIK3R3
1 1 46098008 intron variant C/A snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs10858740
rs10858740 		5 12 88451258 intergenic variant A/G;T snv 0.56 0.700 1.000 1 2019 2019
dbSNP: rs10883710
rs10883710
PPRC1
1 10 102125800 intergenic variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10910476
rs10910476 		2 1 234599210 regulatory region variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10928378
rs10928378
MBD5
1 2 148170400 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10964704
rs10964704
FOCAD
1 9 20795736 intron variant A/G snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs10971930
rs10971930
DCAF12
1 9 34116085 intron variant T/C snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs10974716
rs10974716
SPATA6L ; PLPP6
2 9 4661574 intron variant C/G snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs11030976
rs11030976
RRM1
1 11 4108629 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs11039624
rs11039624 		1 11 48269014 downstream gene variant G/A snv 2.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs11041699
rs11041699
EIF3F
1 11 7983923 intron variant G/A snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs11042023
rs11042023
TRIM66
3 1.000 0.080 11 8640969 missense variant T/C snv 0.60 0.59 0.700 1.000 1 2019 2019
dbSNP: rs1104888
rs1104888
C7orf50 ; LOC107986755
1 7 1066376 intron variant G/T snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs1107960
rs1107960 		2 14 54917622 intergenic variant T/A snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs11082498
rs11082498
EPG5
2 1.000 0.080 18 45922762 intron variant T/C snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs11106996
rs11106996
LOC643339
1 12 93367047 intron variant C/T snv 0.14 0.700 1.000 1 2019 2019