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: rs17211233
rs17211233
RASGRF2
4 0.882 0.040 5 81072944 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs55945116
rs55945116
SEC11A
4 0.882 0.040 15 84676882 intron variant G/C snv 0.26 0.700 1.000 1 2018 2018