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: rs1131690795
rs1131690795
1 1.000 0.160 11 32434769 frameshift variant C/- delins 0.700 0
dbSNP: rs121907911
rs121907911
1 1.000 0.160 11 32434815 stop gained G/T snv 0.700 0
dbSNP: rs1554946500
rs1554946500
4 0.851 0.280 11 32434883 stop gained G/A snv 0.700 0
dbSNP: rs1554946600
rs1554946600
4 0.851 0.280 11 32435027 frameshift variant C/- delins 0.700 0
dbSNP: rs1565000973
rs1565000973
4 0.851 0.280 11 32434708 frameshift variant C/- del 0.700 0
dbSNP: rs1565001383
rs1565001383
2 0.925 0.200 11 32434889 stop gained C/A snv 0.700 0
dbSNP: rs1049509674
rs1049509674
2 0.925 0.200 11 32435341 missense variant T/C snv 0.010 1.000 1 2002 2002
dbSNP: rs2301254
rs2301254
3 0.882 0.160 11 32436129 intron variant A/G snv 0.48 0.010 1.000 1 2005 2005
dbSNP: rs6508
rs6508
3 0.882 0.160 11 32438918 non coding transcript exon variant G/A snv 8.3E-02 0.16 0.010 1.000 1 2005 2005