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: rs114714860
rs114714860
ULK4
1 3 41841413 intron variant G/C snv 0.33 0.700 1.000 1 2017 2017
dbSNP: rs115234772
rs115234772 		1 2 53423157 TF binding site variant A/G snv 3.7E-03 0.700 1.000 1 2018 2018
dbSNP: rs1152958
rs1152958
MYRFL ; PRANCR
1 12 69931889 intron variant G/A snv 0.26 0.700 1.000 1 2017 2017
dbSNP: rs115726563
rs115726563 		1 6 31098642 intergenic variant C/T snv 0.700 1.000 1 2017 2017
dbSNP: rs116008367
rs116008367
ACOXL ; MIR4435-2HG
1 2 111049969 intron variant G/C snv 5.0E-03 0.700 1.000 1 2018 2018
dbSNP: rs11628933
rs11628933 		1 14 60234185 intergenic variant G/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs11631778
rs11631778
THSD4
1 15 71314041 intron variant G/A snv 0.59 0.700 1.000 1 2017 2017
dbSNP: rs11665020
rs11665020
PIEZO2
1 18 10879505 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs11671323
rs11671323 		1 19 21696775 intergenic variant A/G snv 0.41 0.700 1.000 1 2017 2017
dbSNP: rs11681462
rs11681462 		1 2 42125427 intergenic variant A/C snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs117059939
rs117059939 		1 14 36401137 intron variant G/T snv 9.5E-03 0.700 1.000 1 2017 2017
dbSNP: rs11716531
rs11716531
SLC4A7
1 3 27415717 intron variant G/A snv 0.18 0.700 1.000 1 2017 2017
dbSNP: rs117638970
rs117638970
PAQR5
1 15 69383266 intron variant C/T snv 5.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs11780200
rs11780200 		1 8 119446281 intron variant G/A snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs11923667
rs11923667 		1 3 101549236 regulatory region variant T/A snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs11931572
rs11931572 		1 4 30084482 intergenic variant A/C snv 1.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs12052761
rs12052761
LINC01890
1 2 68838709 upstream gene variant G/A snv 0.42 0.700 1.000 1 2018 2018
dbSNP: rs12078697
rs12078697
LINC01762
1 1 116472496 intron variant G/C snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs12142296
rs12142296
PIK3R3 ; P3R3URF-PIK3R3
1 1 46076007 intron variant T/G snv 9.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs1215469
rs1215469
LOC105370275
1 13 80133273 intron variant A/C snv 0.82 0.700 1.000 1 2018 2018
dbSNP: rs12184466
rs12184466
CCDC63
1 12 110843832 intron variant C/T snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs1220128
rs1220128 		1 2 157643390 intergenic variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs12203179
rs12203179
COL21A1
1 6 56129439 intron variant C/G snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs12208772
rs12208772
LOC105377979
1 6 121804281 intergenic variant T/C snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs12216886
rs12216886
VLDLR-AS1 ; LOC101930053
1 9 2493751 intron variant T/G snv 0.18 0.700 1.000 1 2018 2018