Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs494558
COL4A1
13 110276815 intron variant C/T snv 0.90 2
rs577358806
LINC01822
2 21691067 intron variant C/T snv 1.5E-03 2
rs58231626
PAX8 ; PAX8-AS1
2 113256632 non coding transcript exon variant G/A snv 6.8E-04 2
rs6587515 1 150636412 regulatory region variant G/A snv 7.2E-02 2
rs6864091
POC5
5 75714177 intron variant T/C snv 0.43 2
rs6943127
CALCR
7 93568946 intron variant T/G snv 0.29 2
rs7187961
FTO
16 53792122 intron variant T/C snv 0.86 2
rs761567588
CDYL
6 4790301 intron variant A/G snv 1.3E-04 2
rs7777593 7 36506461 downstream gene variant T/A;G snv 2
rs8062405
ATXN2L
16 28826585 non coding transcript exon variant A/G snv 0.35 2
rs9374842 6 119864519 regulatory region variant C/T snv 0.76 2
rs10782199
LOC105377975
6 119791894 intergenic variant G/A snv 0.32 1
rs112037309
ARHGEF38 ; INTS12
4 105695979 intron variant G/A snv 6.7E-02 1
rs11288989
NIPBL
5 37043527 intron variant AAA/-;A;AA;AAAA;AAAAA delins 1
rs12517906 5 180743819 upstream gene variant C/A;T snv 0.11 1
rs12705992 7 114789947 regulatory region variant G/A snv 0.72 1
rs13029479 2 655222 regulatory region variant G/A snv 0.13 1
rs143814719
LOC105372155
18 60300038 intron variant AAG/- delins 0.21 1
rs151204774 11 21580341 downstream gene variant AATT/- delins 7.4E-02 1
rs16877106
ANAPC4
4 25401644 intron variant C/T snv 4.9E-02 1
rs17109221
NRXN3
14 79443776 intron variant C/T snv 0.21 1
rs182624399 11 70019090 intron variant C/T snv 8.9E-03 1
rs1840440 18 25677222 intergenic variant T/C;G snv 1
rs1973993 1 96478438 intergenic variant T/C snv 0.49 1
rs2256174
MICA
6 31412645 intron variant A/G snv 0.64 1