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: rs1847018
rs1847018
1 1.000 0.040 5 32714555 intron variant C/T snv 0.12 0.010 1.000 1 2015 2015
dbSNP: rs2270915
rs2270915
2 1.000 0.040 5 32786283 missense variant A/C;G;T snv 0.21 0.18 0.010 1.000 1 2017 2017