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: rs113851554
rs113851554
MEIS1
5 0.882 0.080 2 66523432 intron variant G/A;T snv 0.010 1.000 1 2018 2018
dbSNP: rs12469063
rs12469063
MEIS1
2 0.925 0.080 2 66537176 intron variant A/G snv 0.18 0.010 1.000 1 2018 2018
dbSNP: rs2300478
rs2300478
MEIS1
6 0.851 0.120 2 66554321 intron variant T/G snv 0.21 0.010 1.000 1 2018 2018