Gene: LINC01004 ×
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: rs34180096
rs34180096
KMT2E ; LINC01004
1 7 104968145 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs56016333
rs56016333
KMT2E ; LINC01004
2 7 104955801 intron variant T/C snv 0.30 0.700 1.000 1 2018 2018
dbSNP: rs7776707
rs7776707
KMT2E ; LINC01004
2 1.000 0.040 7 104965083 intron variant C/A snv 0.31 0.700 1.000 1 2019 2019