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: rs113994027
rs113994027
1 1.000 0.040 2 27368047 missense variant G/A snv 0.700 0
dbSNP: rs113994028
rs113994028
1 1.000 0.040 2 27368104 missense variant C/A;T snv 2.7E-05 2.8E-05 0.700 0
dbSNP: rs113994031
rs113994031
1 1.000 0.040 2 27367536 missense variant A/C;G snv 2.0E-05 2.1E-05 0.700 0
dbSNP: rs113994035
rs113994035
1 1.000 0.040 2 27366830 missense variant G/A snv 6.8E-05 7.0E-05 0.700 0
dbSNP: rs113994037
rs113994037
1 1.000 0.040 2 27366758 splice donor variant C/T snv 0.700 0
dbSNP: rs113994038
rs113994038
2 0.925 0.120 2 27364579 missense variant A/G snv 1.4E-05 0.700 0
dbSNP: rs113994040
rs113994040
2 0.925 0.120 2 27364507 missense variant A/G snv 4.0E-06 7.0E-06 0.700 0
dbSNP: rs1347693309
rs1347693309
1 1.000 0.040 2 27367777 missense variant C/T snv 7.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs1406758215
rs1406758215
1 1.000 0.040 2 27364864 missense variant A/G snv 7.0E-06 0.010 1.000 1 2015 2015