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: rs12930850
rs12930850
CMIP
1 16 81568607 intron variant A/G snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs12972366
rs12972366
UHRF1
1 19 4920402 intron variant A/G snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs12978472
rs12978472
INSR
5 19 7257979 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs13021222
rs13021222 		1 2 164191395 intron variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs13108218
rs13108218
HGFAC
7 4 3442204 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs13125101
rs13125101 		6 4 80253438 TF binding site variant G/A snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs13127398
rs13127398
BANK1
1 4 102000547 intron variant T/A snv 4.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs13179413
rs13179413
C5orf67
2 5 56572270 intron variant C/T snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs13190036
rs13190036
MXD3
1 5 177310719 non coding transcript exon variant A/G snv 0.83 0.89 0.700 1.000 1 2019 2019
dbSNP: rs13210511
rs13210511 		2 6 126834566 intron variant C/T snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs13265769
rs13265769 		1 8 81912028 intron variant T/C snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs13285624
rs13285624
ZCCHC7
1 9 37129499 intron variant T/G snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs13358657
rs13358657 		1 5 158511062 intron variant A/G snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs134557
rs134557
C22orf31
1 22 29061594 intron variant A/G;T snv 0.84 0.700 1.000 1 2019 2019
dbSNP: rs1367117
rs1367117
APOB
8 1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 0.700 1.000 1 2019 2019
dbSNP: rs138922864
rs138922864
CLUAP1
1 16 3527279 intron variant C/G snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs139491786
rs139491786
SLC9A3R2
4 16 2036420 missense variant C/T snv 3.4E-03 3.5E-03 0.700 1.000 1 2019 2019
dbSNP: rs140570886
rs140570886
LPA
3 1.000 0.040 6 160591981 intron variant T/C snv 2.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs142076278
rs142076278 		1 16 51794418 intergenic variant A/G snv 9.5E-03 0.700 1.000 1 2019 2019
dbSNP: rs1436138
rs1436138
SEPTIN9
2 17 77320798 intron variant A/G snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs1440371
rs1440371
LINC01169
2 15 66648746 intron variant G/A snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs145158522
rs145158522
SORCS3
1 10 104870101 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs150532297
rs150532297 		1 5 158169198 downstream gene variant G/A snv 4.1E-03 0.700 1.000 1 2019 2019
dbSNP: rs1507151
rs1507151 		1 6 78773529 intergenic variant T/C snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs1581717
rs1581717
PKHD1
1 6 51969222 intron variant C/A snv 0.38 0.700 1.000 1 2019 2019