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: rs2395607
rs2395607
2 6 34805950 intron variant C/T snv 0.22 0.700 1.000 1 2017 2017
dbSNP: rs9469913
rs9469913
2 6 34859308 missense variant A/G;T snv 4.0E-06; 0.16 0.700 1.000 1 2017 2017