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: rs1555446980
rs1555446980
2 1.000 15 96332169 stop gained C/T snv 0.700 1.000 10 1999 2017
dbSNP: rs1555447237
rs1555447237
2 1.000 15 96334573 missense variant T/C snv 0.700 1.000 10 1999 2017