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: rs1448903
rs1448903
ADAM23
1 2 206444237 intron variant A/G snv 6.1E-02 0.700 1.000 3 2018 2019
dbSNP: rs1018454
rs1018454
DPT
1 1 168728523 intron variant A/C snv 0.57 0.700 1.000 2 2018 2018
dbSNP: rs10405357
rs10405357
LILRB5
1 19 54255803 intron variant T/C snv 0.50 0.700 1.000 2 2018 2018
dbSNP: rs10490666
rs10490666
VIT
1 2 36705350 intron variant A/T snv 0.26 0.700 1.000 2 2018 2018
dbSNP: rs10509554
rs10509554
LIPN
1 10 88766035 intron variant C/T snv 0.26 0.700 1.000 2 2018 2018
dbSNP: rs1147707
rs1147707
FSTL1
1 3 120450401 intron variant C/T snv 0.28 0.700 1.000 2 2018 2018
dbSNP: rs11581248
rs11581248
SLAMF7
1 1 160750284 intron variant C/T snv 8.7E-02 8.6E-02 0.700 1.000 2 2018 2018
dbSNP: rs13318853
rs13318853
CPB1
1 3 148844612 intron variant G/A;T snv 0.22; 4.0E-06 0.700 1.000 2 2018 2018
dbSNP: rs139695917
rs139695917
GXYLT1
1 12 42133239 intron variant T/C snv 7.8E-03 0.700 1.000 2 2018 2018
dbSNP: rs1468810
rs1468810
VIT
1 2 36766797 intron variant C/A snv 0.45 0.700 1.000 2 2018 2018
dbSNP: rs16837641
rs16837641
NRP2
1 2 205770145 intron variant G/A snv 0.29 0.700 1.000 2 2018 2018
dbSNP: rs16933084
rs16933084
C1S
1 12 7064780 intron variant A/T snv 0.12 0.700 1.000 2 2018 2018
dbSNP: rs1958078
rs1958078
SMOC1
4 14 69888141 intron variant A/C;G snv 0.700 1.000 2 2018 2018
dbSNP: rs2007272
rs2007272
PIGR
1 1 206940410 intron variant G/C snv 0.35 0.700 1.000 2 2018 2018
dbSNP: rs2271893
rs2271893
LMAN2L
3 0.925 0.040 2 96739703 intron variant G/A snv 0.23 0.700 1.000 2 2018 2018
dbSNP: rs2670014
rs2670014
LOC101929415
1 8 56464222 intron variant C/T snv 0.41 0.700 1.000 2 2018 2018
dbSNP: rs342702
rs342702
GPC5
1 13 91770692 intron variant G/T snv 0.37 0.700 1.000 2 2018 2018
dbSNP: rs3765963
rs3765963
CA6
1 1 8974539 intron variant A/G snv 0.48 0.700 1.000 2 2018 2018
dbSNP: rs4233450
rs4233450
PTGFRN
1 1 116947639 intron variant G/T snv 0.80 0.700 1.000 2 2018 2018
dbSNP: rs4499344
rs4499344
PDCD5
3 19 32582525 intron variant G/A snv 0.46 0.700 1.000 2 2018 2018
dbSNP: rs45543339
rs45543339
LRRC25
1 19 18392384 intron variant C/T snv 0.22 0.700 1.000 2 2018 2018
dbSNP: rs4759076
rs4759076
COPZ1 ; MIR148B
1 12 54336088 intron variant T/C snv 0.42 0.700 1.000 2 2018 2018
dbSNP: rs4859610
rs4859610
ART3
1 4 76079288 intron variant A/G snv 0.67 0.700 1.000 2 2018 2018
dbSNP: rs4987358
rs4987358
SELL ; C1orf112
1 1 169696410 intron variant G/A;T snv 0.700 1.000 2 2018 2018
dbSNP: rs4988235
rs4988235
MCM6
19 0.752 0.400 2 135851076 intron variant G/A;C snv 0.700 1.000 2 2018 2018