MYRF, myelin regulatory factor, 745

N. diseases: 102; N. variants: 44
Disease: Serum albumin measurement ×
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: rs108499
rs108499 		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 		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: rs174534
rs174534 		1.000 0.080 11 61781986 non coding transcript exon variant A/G snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174535
rs174535 		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: rs174536
rs174536 		11 61784455 non coding transcript exon variant A/C snv 0.29
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs174537
rs174537 		0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 2 2012 2013
dbSNP: rs10792318
rs10792318 		11 61763971 intron variant A/G snv 0.19
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11230796
rs11230796 		11 61761795 intron variant T/G snv 0.19
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs149803
rs149803 		11 61771548 synonymous variant C/G;T snv 0.18
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs149804
rs149804 		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: rs174529
rs174529 		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: rs174530
rs174530 		1.000 0.080 11 61779120 non coding transcript exon variant A/G snv 0.30
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs174532
rs174532 		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 		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 		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: rs198421
rs198421 		11 61750765 intron variant G/A snv 0.14
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs198459
rs198459 		11 61757548 non coding transcript exon variant G/A snv 0.15 0.14
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs198467
rs198467 		11 61766436 non coding transcript exon variant T/C snv 0.33
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2269928
rs2269928 		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: rs509360
rs509360 		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: rs547589
rs547589 		11 61767400 intron variant A/C;T snv 0.67
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs55903902
rs55903902 		11 61764519 intron variant A/G snv 0.19
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs579383
rs579383 		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: rs61747222
rs61747222 		11 61781324 missense variant G/A snv 2.2E-02 2.2E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs61896141
rs61896141 		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