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: rs672601307
rs672601307
2 1.000 0.080 15 50490443 missense variant T/C snv 0.800 1.000 1 2017 2017
dbSNP: rs672601308
rs672601308
1 1.000 0.080 15 50490444 missense variant C/G snv 0.800 1.000 1 2017 2017
dbSNP: rs672601311
rs672601311
1 1.000 0.080 15 50490450 missense variant C/G snv 0.800 1.000 1 2017 2017
dbSNP: rs672601306
rs672601306
1 1.000 0.080 15 50490442 inframe deletion TCC/- delins 0.700 0