Gene: MECOM ×
Source: GWASCAT ×
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: rs16853722
rs16853722
MECOM
2 3 169432844 intron variant T/C snv 0.11 0.800 1.000 1 2012 2012
dbSNP: rs16853637
rs16853637
MECOM
1 3 169392231 intron variant G/A snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs76272256
rs76272256
MECOM
2 3 169170324 intron variant C/T snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs76273615
rs76273615
MECOM
1 3 169374250 intron variant A/G snv 0.11 0.700 1.000 1 2018 2018