Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1057519744
rs1057519744
1 1.000 0.040 5 171410542 frameshift variant -/CATG;CCTG;TCAG;TCTG ins 0.700 1.000 1 2009 2009
dbSNP: rs1554138188
rs1554138188
1 1.000 0.040 5 171410541 frameshift variant -/CATG;CGTG delins 0.700 0
dbSNP: rs1554138189
rs1554138189
1 1.000 0.040 5 171410540 frameshift variant -/CCTG delins 0.700 0
dbSNP: rs1561878500
rs1561878500
1 1.000 0.040 5 171410549 frameshift variant GGAGGAA/CCCTGGCTAGG delins 0.700 0
dbSNP: rs587776806
rs587776806
1 1.000 0.040 5 171410539 frameshift variant -/TCTG delins 0.700 0