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: rs10428766
rs10428766 		1 6 150052058 intergenic variant C/T snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs10455025
rs10455025
TSLP
3 1.000 0.080 5 111069301 upstream gene variant A/C snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs10471939
rs10471939 		1 5 55180855 intergenic variant T/A snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs10473333
rs10473333 		1 5 43866494 intergenic variant T/A snv 6.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs10481172
rs10481172
CCDC26
1 8 128993202 intron variant A/G snv 0.69 0.700 1.000 1 2019 2019
dbSNP: rs10508366
rs10508366 		1 10 8735729 intergenic variant C/T snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs10542411
rs10542411 		2 2 61541105 upstream gene variant ATATT/-;ATATTATATT delins 0.23 0.700 1.000 1 2016 2016
dbSNP: rs1057258
rs1057258
INPP5D
3 2 233206983 3 prime UTR variant C/T snv 0.30 0.700 1.000 2 2016 2019
dbSNP: rs1059091
rs1059091
IFITM2
1 11 309127 missense variant A/C;G;T snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs1059513
rs1059513
NAB2 ; STAT6
11 0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 0.700 1.000 1 2016 2016
dbSNP: rs1061407
rs1061407
GLDC
1 9 6532544 3 prime UTR variant G/A snv 0.68 0.700 1.000 1 2019 2019
dbSNP: rs10667251
rs10667251 		4 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 0.700 1.000 1 2016 2016
dbSNP: rs1071849
rs1071849
CD52 ; UBXN11
1 1 26320235 missense variant A/G snv 0.67 0.70 0.700 1.000 1 2019 2019
dbSNP: rs10767658
rs10767658
BDNF-AS
2 11 27650705 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10774624
rs10774624
LINC02356
6 0.882 0.160 12 111395984 intron variant G/A snv 0.67 0.700 1.000 1 2019 2019
dbSNP: rs10777163
rs10777163
POC1B
1 12 89436943 intron variant T/C snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs10794666
rs10794666
RUNX3 ; LOC107984932
1 1 24924339 intron variant C/T snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs10795656
rs10795656 		4 1.000 0.080 10 8553876 intergenic variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10810657
rs10810657 		7 0.827 0.080 9 16884588 regulatory region variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs10822220
rs10822220 		1 10 63841301 intron variant A/G snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs10852622
rs10852622
ZFPM1
2 16 88490472 intron variant A/G snv 0.35 0.700 1.000 1 2016 2016
dbSNP: rs10858740
rs10858740 		5 12 88451258 intergenic variant A/G;T snv 0.56 0.700 1.000 1 2016 2016
dbSNP: rs10864462
rs10864462
PEX14
1 1 10552101 intron variant A/T snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs10882899
rs10882899
FRAT2 ; LOC105378448
1 10 97336188 intron variant G/C snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs10893844
rs10893844 		2 11 128315955 regulatory region variant G/C snv 0.36 0.700 1.000 2 2016 2019