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: rs11618432
rs11618432
1 13 46120581 non coding transcript exon variant T/G snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs1926446
rs1926446
1 13 46055860 intron variant C/A;G snv 0.73 0.700 1.000 1 2018 2018
dbSNP: rs1926447
rs1926447
11 0.807 0.440 13 46055809 missense variant A/G snv 0.74 0.77 0.700 1.000 1 2018 2018
dbSNP: rs35814191
rs35814191
1 13 46107376 intron variant C/- delins 0.34 0.700 1.000 1 2018 2018
dbSNP: rs4942471
rs4942471
1 13 46070358 intron variant C/T snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs532540191
rs532540191
1 13 46055075 intron variant AAA/-;A;AA;AAAA;AAAAA delins 0.74 0.700 1.000 1 2018 2018
dbSNP: rs9526137
rs9526137
1 13 46067114 intron variant A/G snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs9526138
rs9526138
1 13 46067128 intron variant G/C;T snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs9567617
rs9567617
1 13 46076973 intron variant C/G snv 0.34 0.700 1.000 1 2018 2018