WT1-AS, WT1 antisense RNA, 51352

N. diseases: 71; N. variants: 16
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: rs2301254
rs2301254 		0.882 0.160 11 32436129 intron variant A/G snv 0.48
CUI: C0017668
Disease: Focal glomerulosclerosis
Focal glomerulosclerosis 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2005 2005
dbSNP: rs2301254
rs2301254 		0.882 0.160 11 32436129 intron variant A/G snv 0.48
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection 		0.010 1.000 1 2005 2005
dbSNP: rs3809060
rs3809060 		11 32437261 intron variant G/T snv 0.49
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs3809060
rs3809060 		11 32437261 intron variant G/T snv 0.49
CUI: C0019294
Disease: Hernia, Inguinal
Hernia, Inguinal 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2015 2015
dbSNP: rs6508
rs6508 		0.882 0.160 11 32438918 non coding transcript exon variant G/A snv 8.3E-02 0.16
CUI: C0017668
Disease: Focal glomerulosclerosis
Focal glomerulosclerosis 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2005 2005
dbSNP: rs6508
rs6508 		0.882 0.160 11 32438918 non coding transcript exon variant G/A snv 8.3E-02 0.16
CUI: C2363741
Disease: HIV-1 infection
HIV-1 infection 		0.010 1.000 1 2005 2005
dbSNP: rs6508
rs6508 		0.882 0.160 11 32438918 non coding transcript exon variant G/A snv 8.3E-02 0.16
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2005 2005