Gene: MYLIP ×
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: rs3757354
rs3757354
MYLIP
3 6 16127176 upstream gene variant C/T snv 0.27 0.800 1.000 5 2010 2019
dbSNP: rs2235215
rs2235215
MYLIP
2 6 16130925 intron variant T/C snv 0.46 0.700 1.000 1 2019 2019