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: rs104893620
rs104893620
6 0.851 0.120 2 98395999 missense variant C/T snv 9.5E-05 7.0E-05 0.700 0
dbSNP: rs1555968941
rs1555968941
31 0.752 0.280 12 2653847 missense variant G/A;C snv 0.700 0
dbSNP: rs1558811557
rs1558811557
5 0.851 0.120 2 98377710 frameshift variant -/TCAGTGCTGCAGCCGGGGATCG delins 0.700 0
dbSNP: rs267607261
rs267607261
28 0.807 0.280 2 27312753 stop gained C/T snv 8.0E-06 0.700 0
dbSNP: rs368900406
rs368900406
27 0.827 0.160 2 27312255 non coding transcript exon variant A/C snv 8.0E-06 2.1E-05 0.700 0
dbSNP: rs122468178
rs122468178
5 0.851 0.320 X 21880921 missense variant G/A snv 0.010 1.000 1 2012 2012
dbSNP: rs267607077
rs267607077
4 0.882 0.080 2 96287968 missense variant G/A snv 4.0E-06 0.010 1.000 1 2019 2019