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: rs108499
rs108499
MYRF ; TMEM258
11 61779765 intron variant C/T snv 0.27
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174528
rs174528
MYRF ; TMEM258
1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 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: rs149804
rs149804
MYRF ; TMEM258
11 61771134 intron variant A/G snv 0.31
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
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: rs174529
rs174529
MYRF ; TMEM258
11 61776489 intron variant T/C snv 0.34
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
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: rs174532
rs174532
MYRF ; TMEM258
11 61781402 intron variant G/A snv 0.20
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs174533
rs174533
MYRF ; TMEM258
0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs17762402
rs17762402
MYRF ; TMEM258
11 61785729 intron variant G/A snv 4.8E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
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: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
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: rs509360
rs509360
MYRF ; TMEM258
11 61781087 intron variant A/G snv 0.61 0.52
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
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: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
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: rs61896141
rs61896141
MYRF ; TMEM258
11 61788567 intron variant A/C snv 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs628993
rs628993
MYRF ; TMEM258
11 61772219 intron variant G/A snv 8.8E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs650436
rs650436
MYRF ; TMEM258
11 61768958 intron variant C/T snv 0.39
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
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
dbSNP: rs695867
rs695867
TMEM258 ; FEN1 ; FADS2 ; MIR611
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: rs7943728
rs7943728
MYRF ; TMEM258
1.000 0.080 11 61779596 intron variant G/A snv 0.12 0.11
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin 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: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174535
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012