Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2182885
UBAC2
13 99202870 intron variant G/A snv 0.46 2
rs34675278 5 98808491 intergenic variant AA/-;A;AAA;AAAA;AAAAA delins 2
rs397933924 10 97314229 upstream gene variant -/CAGGTTCAAGCGA ins 5
rs36058533 2 96570916 intergenic variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTTTT delins 2
rs72079386 2 96565882 intergenic variant GCTT/-;GCTTGCTT delins 0.32 2
rs11555542
ASB2
14 93951185 missense variant T/C snv 3.3E-02 3.7E-02 2
rs797680
CCDC18
1 93251417 intron variant G/A;T snv 2
rs2072735
SPSB1
1 9295413 intron variant A/C snv 0.76 2
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs8
CDK6
7 92779015 intron variant C/T snv 0.14 2
rs11319879
HHEX
10 92693719 intron variant A/- delins 0.53 2
rs3742716
RIN3
14 92652324 synonymous variant G/A snv 0.32 0.25 2
rs11624512
RIN3
14 92644775 non coding transcript exon variant C/T snv 0.15 5
rs42033
CDK6
0.882 0.080 7 92608219 3 prime UTR variant A/T snv 0.16 5
rs8179
CDK6
0.882 0.080 7 92606850 3 prime UTR variant T/A;C;G snv 8
rs7135535
LINC01619
12 92125513 intron variant G/A snv 0.38 2
rs12762973
LARP4B
10 914821 intron variant C/A;G snv 1
rs201272561
AUH
9 91334470 intron variant C/T snv 4.2E-05 2
rs12264390
LARP4B
10 913171 intron variant T/C snv 0.20 2
rs2010672
CRTC3-AS1
15 90658042 intron variant G/C;T snv 2
rs2074585
IQGAP1
0.925 0.080 15 90466252 intron variant G/A snv 0.63 0.67 5
rs17585295
BACH2
6 90235112 intron variant C/T snv 0.27 2
rs200830364 11 90199744 downstream gene variant AAAAA/-;A;AA;AAA;AAAA;AAAAAA delins 0.38 1
rs11018874
NAALAD2
11 90142269 intron variant G/A snv 9.7E-02 2
rs61840192 1.000 0.080 10 9001441 intergenic variant G/A;C;T snv 3