Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10404486
rs10404486
19 52780882 non coding transcript exon variant C/T snv 0.20
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs10517480
rs10517480
4 59883111 intergenic variant A/T snv 0.27
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2008 2008
dbSNP: rs1061808
rs1061808
6 32168770 3 prime UTR variant T/G snv 0.64
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs10769780
rs10769780
11 7345864 intron variant T/C snv 0.25
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs10885997
rs10885997
10 116638460 synonymous variant A/G snv 0.38 0.36
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs11662721
rs11662721
18 21681452 intron variant C/T snv 0.15
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs11667159
rs11667159
19 46291989 intergenic variant C/A;T snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2017 2017
dbSNP: rs11668290
rs11668290
19 46292921 upstream gene variant G/A snv 0.12
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2017 2017
dbSNP: rs11671319
rs11671319
19 46291810 intergenic variant T/C snv 0.12
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2017 2017
dbSNP: rs11671360
rs11671360
19 46291914 intergenic variant T/C snv 0.12
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2017 2017
dbSNP: rs11671710
rs11671710
19 46288677 regulatory region variant C/G;T snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2017 2017
dbSNP: rs117366905
rs117366905
19 46294033 upstream gene variant A/G snv 0.12
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2017 2017
dbSNP: rs117992292
rs117992292
19 46294038 upstream gene variant A/G snv 0.12
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2017 2017
dbSNP: rs12423247
rs12423247
12 96464584 intron variant A/T snv 9.2E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs12472274
rs12472274
2 238186781 non coding transcript exon variant G/A;T snv
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs138572223
rs138572223
18 50446052 intergenic variant A/G snv 5.7E-03
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2017 2017
dbSNP: rs139368489
rs139368489
18 50502045 intergenic variant T/C snv 5.8E-03
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2017 2017
dbSNP: rs141332218
rs141332218
19 46293976 upstream gene variant T/C snv 0.12
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2017 2017
dbSNP: rs1424760
rs1424760
2 162925277 intergenic variant C/T snv 0.52
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs142815467
rs142815467
19 46291277 intergenic variant -/T delins 0.12
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2017 2017
dbSNP: rs146524044
rs146524044
18 50057046 intron variant A/C snv 1.0E-03
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2017 2017
dbSNP: rs151159962
rs151159962
18 50386938 intron variant T/C snv 1.3E-03
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2017 2017
dbSNP: rs17148090
rs17148090
11 85306432 intron variant A/C;G snv 7.4E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs17718828
rs17718828
13 74553977 non coding transcript exon variant C/T snv 8.8E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 1 2012 2012
dbSNP: rs184392658
rs184392658
20 45438925 intron variant T/C snv 3.0E-03
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2017 2017