MYH9, myosin heavy chain 9, 4627

N. diseases: 196; N. variants: 38
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: rs2032487
rs2032487
0.882 0.080 22 36299382 intron variant C/T snv 0.78
CUI: C0035078
Disease: Kidney Failure
Kidney Failure
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.020 1.000 2 2009 2012
dbSNP: rs3752462
rs3752462
0.827 0.160 22 36314138 splice region variant T/C snv 0.57 0.53
CUI: C0035078
Disease: Kidney Failure
Kidney Failure
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2012 2012
dbSNP: rs4821480
rs4821480
0.807 0.160 22 36299201 intron variant G/T snv 0.78
CUI: C0035078
Disease: Kidney Failure
Kidney Failure
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2009 2009
dbSNP: rs4821481
rs4821481
1.000 0.080 22 36299896 intron variant C/T snv 0.78
CUI: C0035078
Disease: Kidney Failure
Kidney Failure
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2009 2009