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: rs672601376
rs672601376
3 0.925 0.040 12 13608760 missense variant A/C snv 0.010 1.000 1 2014 2014
dbSNP: rs672601378
rs672601378
4 0.882 0.040 12 13615149 missense variant C/T snv 0.010 1.000 1 2014 2014