Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7107916
SBF2
11 9990964 intron variant A/G snv 0.27 1
rs10786559 10 99549133 intergenic variant G/C;T snv 1
rs11190134 10 99522443 upstream gene variant G/A snv 0.36 3
rs7078219 10 99514608 intergenic variant G/A snv 0.38 1
rs7095491 10 99514301 intergenic variant T/C snv 0.50 1
rs13260338
VPS13B
8 99338516 intron variant T/C snv 6.0E-02 1
rs7855251
TRIM14
9 98105907 intron variant T/C snv 0.35 1
rs10985065
TRIM14
9 98104621 intron variant C/G;T snv 1
rs7022455
TRIM14
9 98104590 intron variant T/C snv 0.35 1
rs1031868 8 97627834 upstream gene variant A/G snv 0.11 2
rs415895
SWAP70
11 9748015 missense variant C/G snv 0.62 0.61 6
rs2562177
NPRL3
16 95284 intron variant C/T snv 6.1E-02 1
rs6600233
NPRL3
16 93505 intron variant C/G;T snv 3
rs2541618
NPRL3
16 92827 non coding transcript exon variant T/C snv 0.84 1
rs2562181
NPRL3
16 91661 intron variant C/T snv 0.12 1
rs11042154
LOC105376541
11 9008153 intron variant G/A snv 0.32 1
rs6486060
NRIP3 ; LOC105376541
11 9003083 intron variant G/A snv 0.55 2
rs7930026
NRIP3
11 8992092 intron variant T/A;C snv 1
rs7925728
NRIP3
11 8991455 intron variant A/G snv 0.56 1
rs11042149
NRIP3
11 8989190 intron variant T/C snv 0.49 1
rs10769979
NRIP3
11 8989112 intron variant G/A;T snv 1
rs1980428
NRIP3
11 8988950 intron variant C/T snv 0.49 1
rs1980429
NRIP3
11 8988927 intron variant C/A;T snv 1
rs1123936
NRIP3
11 8981759 3 prime UTR variant A/G snv 0.51 1
rs2742480
TMEM9B-AS1
11 8971583 intron variant A/G snv 0.54 1