Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1058694
rs1058694
21 43984239 3 prime UTR variant C/T snv 0.32
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs7435
rs7435
21 43984457 3 prime UTR variant A/G snv 0.35
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs78512431
rs78512431
1.000 21 43970856 intron variant T/A;C snv 0.10
Adverse effects, not elsewhere classified
0.700 1.000 1 2019 2019