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: rs35262860
rs35262860
RP1
1 8 54566349 intron variant -/CT delins 0.31 0.700 1.000 1 2019 2019
dbSNP: rs10256972
rs10256972
C7orf50
1 7 999367 intron variant A/C snv 0.62 0.800 1.000 1 2010 2010
dbSNP: rs4732038
rs4732038
AKR1B15
1 7 134565570 intron variant A/C snv 0.51 0.52 0.800 1.000 1 2010 2010
dbSNP: rs9517320
rs9517320
STK24
1 13 98474049 intron variant A/C snv 0.55 0.800 1.000 1 2010 2010
dbSNP: rs9664222
rs9664222 		1 10 87578876 intergenic variant A/C snv 0.84 0.800 1.000 1 2010 2010
dbSNP: rs2069837
rs2069837
IL6 ; IL6-AS1
18 0.724 0.520 7 22728408 intron variant A/C;G snv 0.700 1.000 2 2016 2019
dbSNP: rs2075650
rs2075650
TOMM40
45 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.800 1.000 2 2011 2012
dbSNP: rs4420638
rs4420638
APOC1
43 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 0.800 1.000 2 2011 2014
dbSNP: rs1950902
rs1950902
MTHFD1
11 0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 0.700 1.000 1 2018 2018
dbSNP: rs2031577
rs2031577 		1 10 4007811 intergenic variant A/G snv 0.53 0.800 1.000 1 2010 2010
dbSNP: rs2229188
rs2229188
CYP51A1 ; CYP51A1-AS1
1 7 92134309 missense variant A/G snv 4.3E-06 0.700 1.000 1 2015 2015
dbSNP: rs4721135
rs4721135
MAD1L1
1 7 1872586 intron variant A/G snv 0.37 0.800 1.000 1 2010 2010
dbSNP: rs5766691
rs5766691
TBC1D22A
1 22 47136753 intron variant A/G snv 0.73 0.800 1.000 1 2010 2010
dbSNP: rs1262476
rs1262476
LOC105377992
2 6 126665850 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs6915183
rs6915183 		1 6 166292681 intergenic variant A/G;T snv 0.800 1.000 1 2010 2010
dbSNP: rs7039467
rs7039467
CDKN2B-AS1
1 9 22056214 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs9876781
rs9876781
CCDC51 ; ATRIP ; ATRIP-TREX1
1 3 48445934 intron variant A/G;T snv 0.800 1.000 1 2010 2010
dbSNP: rs9841144
rs9841144
CADM2
1 3 85482049 intron variant A/T snv 0.17 0.700 1.000 1 2015 2015
dbSNP: rs432203
rs432203
TGFA
1 2 70537556 intron variant C/A snv 0.58 0.800 1.000 1 2010 2010
dbSNP: rs7168365
rs7168365
WDR72 ; LOC105370826
1 15 53513628 downstream gene variant C/A snv 0.37 0.800 1.000 1 2010 2010
dbSNP: rs2440012
rs2440012
ANKRD20A9P
1 13 18865983 intron variant C/A;G snv 0.700 1.000 1 2016 2016
dbSNP: rs7894051
rs7894051
ECHS1
1 10 133370917 intron variant C/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs2882281
rs2882281 		1 13 89970201 intergenic variant C/A;G;T snv 0.800 1.000 1 2010 2010
dbSNP: rs10445407
rs10445407
SLC38A10
1 17 81288009 intron variant C/A;T snv 0.800 1.000 1 2010 2010
dbSNP: rs3847687
rs3847687
ADGRD1
1 12 131040508 intron variant C/A;T snv 0.35 0.800 1.000 1 2010 2010