Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1064795577 1.000 13 32337627 stop gained T/A snv 1
rs1064795578 1.000 13 32363200 frameshift variant A/- delins 1
rs1064795652 1.000 13 32339465 stop gained A/G;T snv 1
rs1064795789 1.000 13 32339948 frameshift variant A/- del 1
rs1064795851 1.000 13 32394756 frameshift variant C/- delins 1
rs1064795884 1.000 13 32356447 frameshift variant GCCAGAGATATACAGGATATGCGAAT/- delins 1
rs1064795934 1.000 13 32336628 frameshift variant G/- del 1
rs1064796073 1.000 13 32333311 frameshift variant A/- del 1
rs1085308035 1.000 13 32319302 stop gained T/G snv 1
rs1085308037 1.000 13 32341005 frameshift variant AAGAT/- del 1
rs1085308038 1.000 13 32341007 frameshift variant G/- del 1
rs1228762581 1.000 13 32336263 splice acceptor variant A/T snv 1
rs138734772 1.000 13 32333072 stop gained G/A;C;T snv 8.1E-06; 4.0E-06 1
rs145988146 1.000 13 32319282 stop gained C/A;G;T snv 1.2E-05 1
rs1555280053 1.000 13 32316420 splice acceptor variant A/G snv 1
rs1555280367 1.000 13 32319180 frameshift variant C/- del 1
rs1555280388 1.000 13 32319232 frameshift variant -/A ins 1
rs1555280427 1.000 13 32319284 frameshift variant -/CCAT ins 1
rs1555280954 1.000 13 32326140 frameshift variant -/T ins 1
rs1555280989 1.000 13 32326253 frameshift variant -/G delins 1
rs1555281000 1.000 13 32326281 frameshift variant -/C ins 1
rs1555281066 1.000 13 32326545 frameshift variant -/G delins 1
rs1555281068 1.000 13 32326550 frameshift variant -/AACG ins 1
rs1555281101 1.000 13 32326595 frameshift variant -/TGAG ins 1
rs1555281102 1.000 13 32326594 stop gained -/TGAG ins 1