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: rs143141689
rs143141689
3 0.882 0.280 1 52397773 missense variant C/T snv 9.5E-05 1.6E-04 0.010 1.000 1 2015 2015
dbSNP: rs374279734
rs374279734
2 0.925 0.280 8 61653585 missense variant T/C snv 8.0E-06 4.2E-05 0.010 1.000 1 2015 2015
dbSNP: rs775266057
rs775266057
1 1.000 0.080 8 116847532 missense variant C/T snv 8.0E-06 0.800 1.000 1 2015 2015
dbSNP: rs387906842
rs387906842
2 0.925 0.080 17 40294388 missense variant C/G;T snv 0.010 1.000 1 2017 2017
dbSNP: rs1437544261
rs1437544261
2 0.925 0.280 21 33581303 missense variant T/C snv 7.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs774052186
rs774052186
2 0.925 0.280 21 33584744 missense variant G/A snv 0.010 1.000 1 2019 2019