Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2018985 2 233740214 intron variant A/G snv 0.47 3
rs2070959 0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 3
rs2741034 2 233640168 intron variant A/G snv 0.22 3
rs3806597 2 233728923 intron variant A/G snv 0.56 3
rs4294999 2 233726821 intron variant A/G snv 0.54 3
rs4553819 2 233685437 intron variant A/G snv 0.39 3
rs6431628 2 233738832 intron variant A/G snv 0.56 3
rs6741669 2 233744546 intron variant A/G snv 0.55 3
rs7574296 2 233729603 synonymous variant A/G snv 0.49 0.54 3
rs929596 0.925 0.040 2 233765830 intron variant A/G snv 0.32 3
rs10841712 12 20933449 intron variant A/G snv 0.47 2
rs10929251 1.000 0.080 2 233637583 intron variant A/G snv 0.13 2
rs11045598 12 20918279 intron variant A/G snv 0.14 2
rs11045626 12 20965963 intron variant A/G snv 0.14 2
rs11045885 12 21233084 intron variant A/G snv 0.22 2
rs1105880 2 233693319 synonymous variant A/G snv 0.35 0.35 2
rs11563250 2 233774704 upstream gene variant A/G snv 0.11 2
rs11676072 2 233717337 intron variant A/G snv 3.0E-02 2
rs11695484 2 233745803 intron variant A/G snv 0.30 2
rs11890203 2 233871485 upstream gene variant A/G snv 0.14 2
rs11903524 2 233785123 intron variant A/G snv 0.79 2
rs12053462 2 233678993 intron variant A/G snv 0.18 2
rs12317268 12 21199607 intron variant A/G snv 0.18 2
rs12366582 12 21238674 intron variant A/G snv 0.18 2
rs12472244 2 233558197 intron variant A/G snv 0.19 2