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: rs724159948
rs724159948
7 1.000 21 37490273 stop gained C/T snv 0.700 0
dbSNP: rs724159949
rs724159949
15 0.827 0.240 21 37486563 stop gained C/T snv 0.700 0
dbSNP: rs724159950
rs724159950
6 1.000 0.200 21 37486571 frameshift variant TGAG/GAA delins 0.700 0
dbSNP: rs724159951
rs724159951
6 21 37493101 missense variant T/C snv 0.700 0
dbSNP: rs724159952
rs724159952
6 21 37490451 frameshift variant -/G delins 0.700 0
dbSNP: rs724159953
rs724159953
7 1.000 21 37505352 stop gained C/T snv 0.700 0
dbSNP: rs724159954
rs724159954
6 21 37490353 frameshift variant -/A delins 0.700 0
dbSNP: rs724159955
rs724159955
6 1.000 21 37512002 missense variant C/A snv 0.700 0
dbSNP: rs724159956
rs724159956
6 21 37496249 frameshift variant -/G delins 0.700 0