Gene: MECOM ×
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: rs4955665
rs4955665
MECOM
1 3 169637231 intron variant T/C snv 0.42 0.700 1.000 2 2018 2018
dbSNP: rs34781085
rs34781085
MECOM
1 3 169646811 intron variant T/C snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs73174309
rs73174309
MECOM
1 3 169477878 intron variant C/T snv 0.20 0.700 1.000 1 2018 2018