Gene: MCF2L ×
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: rs1046205
rs1046205
MCF2L
1 13 113097743 3 prime UTR variant A/T snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs117989138
rs117989138
MCF2L
1 13 113043357 non coding transcript exon variant G/A snv 1.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs2480952
rs2480952
MCF2L
1 13 113098925 3 prime UTR variant T/C snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs36086577
rs36086577
MCF2L
1 13 113074184 intron variant C/A snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs71446935
rs71446935
MCF2L
1 13 113080062 intron variant A/G snv 0.700 1.000 1 2019 2019