Source: GWASDB

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: rs174537
rs174537
MYRF ; TMEM258
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.800 1.000 1 2014 2019
dbSNP: rs102275
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.810 1.000 1 2010 2018
dbSNP: rs174537
rs174537
MYRF ; TMEM258
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement 		0.700 1.000 1 2012 2012
dbSNP: rs174537
rs174537
MYRF ; TMEM258
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28
CUI: C1261430
Disease: Fasting blood sugar result
Fasting blood sugar result 		0.700 1.000 1 2012 2012
dbSNP: rs102275
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 1 2010 2012
dbSNP: rs174535
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs102275
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs174535
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs174534
rs174534
MYRF ; TMEM258
1.000 0.080 11 61781986 non coding transcript exon variant A/G snv 0.28
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.700 1.000 1 2011 2011
dbSNP: rs102275
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.800 1.000 1 2010 2010
dbSNP: rs102275
rs102275
TMEM258
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
MYRF ; TMEM258
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
MYRF ; TMEM258
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
MYRF ; TMEM258
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
MYRF ; TMEM258
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
MYRF ; TMEM258
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
MYRF ; TMEM258
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
MYRF ; TMEM258
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
TMEM258 ; FEN1 ; MIR611
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
MYRF ; TMEM258
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
MYRF ; TMEM258
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
TMEM258 ; FEN1 ; MIR611
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
MYRF ; TMEM258
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
MYRF ; TMEM258
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
MYRF ; TMEM258
11 61768958 intron variant C/T snv 0.39
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		0.700 1.000 1 2011 2011