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: rs10206089
rs10206089 		4 2 61476184 intron variant G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs10241173
rs10241173 		1 7 124813204 intergenic variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs1025687
rs1025687
MAPK4
3 18 50621423 intron variant T/C snv 0.61 0.700 1.000 1 2016 2016
dbSNP: rs10265538
rs10265538 		2 7 20502242 intergenic variant T/C snv 0.20 0.700 1.000 1 2016 2016
dbSNP: rs10283564
rs10283564
JAK2 ; INSL6
2 9 5075628 intron variant C/G snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs1032726
rs1032726
CD200R1
2 3 112967228 intron variant T/C snv 0.46 0.700 1.000 1 2016 2016
dbSNP: rs10409243
rs10409243
DNMT1 ; S1PR2
6 19 10222312 3 prime UTR variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10410864
rs10410864 		2 19 39711776 downstream gene variant T/C snv 0.68 0.700 1.000 1 2016 2016
dbSNP: rs10428766
rs10428766 		1 6 150052058 intergenic variant C/T snv 0.19 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: rs1059091
rs1059091
IFITM2
1 11 309127 missense variant A/C;G;T snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs1061407
rs1061407
GLDC
1 9 6532544 3 prime UTR variant G/A snv 0.68 0.700 1.000 1 2019 2019
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: 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: 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