TMEM258, transmembrane protein 258, 746

N. diseases: 63; N. variants: 37
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: rs102275
rs102275
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.800 1.000 3 2011 2013
dbSNP: rs108499
rs108499
11 61779765 intron variant C/T snv 0.27
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs149803
rs149803
11 61771548 synonymous variant C/G;T snv 0.18
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174528
rs174528
1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174532
rs174532
11 61781402 intron variant G/A snv 0.20
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174534
rs174534
1.000 0.080 11 61781986 non coding transcript exon variant A/G snv 0.28
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174535
rs174535
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174536
rs174536
11 61784455 non coding transcript exon variant A/C snv 0.29
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs174538
rs174538
0.701 0.440 11 61792609 5 prime UTR variant G/A snv 0.34 0.26
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs17762402
rs17762402
11 61785729 intron variant G/A snv 4.8E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs2269928
rs2269928
11 61770057 intron variant T/G snv 0.18
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs412334
rs412334
11 61792789 5 prime UTR variant C/T snv 0.10
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs509360
rs509360
11 61781087 intron variant A/G snv 0.61 0.52
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs579383
rs579383
11 61769111 intron variant G/A snv 0.58
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs650436
rs650436
11 61768958 intron variant C/T snv 0.39
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs695867
rs695867
11 61793816 intron variant A/G snv 2.6E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs7102974
rs7102974
11 61792563 5 prime UTR variant C/T snv 8.5E-03 9.6E-03
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011
dbSNP: rs740006
rs740006
11 61790396 3 prime UTR variant T/C snv 7.6E-02
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
0.700 1.000 1 2011 2011