Source: ALL
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: rs17112705
rs17112705
ERLIN1
2 10 100177437 intron variant T/C snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs61871700
rs61871700
CPN1
3 10 100068504 intron variant C/A;T snv 0.700 1.000 1 2013 2013