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: rs7934276
rs7934276 		1 11 100631600 regulatory region variant T/C snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs60583266
rs60583266
LINC01349
1 1 100635283 intron variant C/G snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs7385804
rs7385804
TFR2
14 0.851 0.120 7 100638347 intron variant C/A snv 0.65 0.700 1.000 1 2009 2009
dbSNP: rs7141210
rs7141210 		2 14 100716133 regulatory region variant T/C snv 0.55 0.700 1.000 1 2019 2019
dbSNP: rs12088882
rs12088882 		1 1 100759064 intergenic variant C/T snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs2059846
rs2059846
ST8SIA4
1 5 100865206 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs36055153
rs36055153
NPAS2
1 2 100980158 intron variant G/A snv 0.12 0.700 1.000 1 2019 2019
dbSNP: rs733830
rs733830
TBC1D8
1 2 101161857 intron variant T/C snv 0.68 0.700 1.000 1 2019 2019
dbSNP: rs28576226
rs28576226 		1 15 101173463 downstream gene variant G/A snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs57105322
rs57105322
MSRA
1 8 10120812 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs12144133
rs12144133
UBE4B
1 1 10144128 intron variant T/G snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs17041439
rs17041439
SPIC
2 12 101479462 intron variant A/C snv 7.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs6846071
rs6846071
BANK1
2 4 101481058 intron variant T/G snv 0.15 0.700 1.000 1 2013 2013
dbSNP: rs1037117
rs1037117 		1 15 101528455 upstream gene variant G/A snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs6543087
rs6543087
MAP4K4
2 1.000 0.080 2 101699471 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs12787996
rs12787996
YAP1
1 11 102186337 non coding transcript exon variant C/A snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs13135092
rs13135092
SLC39A8
4 4 102276925 intron variant A/G snv 5.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs8113091
rs8113091 		1 19 10239014 intergenic variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs113473633
rs113473633
NFKB1
4 1.000 0.040 4 102527974 intron variant A/G snv 1.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs35879747
rs35879747
SUFU
1 10 102588937 intron variant T/A snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs10883756
rs10883756 		1 10 102640355 upstream gene variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs4807440
rs4807440
CNN2
3 19 1026478 upstream gene variant G/T snv 0.65 0.700 1.000 2 2016 2019
dbSNP: rs7917772
rs7917772
SFXN2
3 10 102727686 3 prime UTR variant G/A;C snv 0.46 0.700 1.000 1 2016 2016
dbSNP: rs2431320
rs2431320
PAM
1 5 102782681 intron variant C/T snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs972142
rs972142 		1 8 102824025 downstream gene variant A/G snv 0.38 0.700 1.000 1 2019 2019