Source: CURATED ×
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: rs757075712
rs757075712
14 0.763 0.200 10 58390856 missense variant C/T snv 1.6E-05 1.4E-05 0.710 1.000 0 2016 2016
dbSNP: rs139194636
rs139194636
6 0.882 0.240 1 119033203 missense variant T/C snv 6.4E-05 2.3E-04 0.700 0
dbSNP: rs367956522
rs367956522
7 0.851 0.240 13 51949798 splice acceptor variant T/C snv 2.4E-05 7.7E-05 0.700 0
dbSNP: rs757600616
rs757600616
6 0.882 0.240 1 119033279 stop gained G/A snv 1.2E-05 0.700 0