Source: ALL

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: rs1799929
rs1799929
0.776 0.240 8 18400484 synonymous variant C/T snv 0.36 0.36
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 1997 1997
dbSNP: rs1799929
rs1799929
0.776 0.240 8 18400484 synonymous variant C/T snv 0.36 0.36
CUI: C0004096
Disease: Asthma
Asthma
0.010 1.000 1 2006 2006
dbSNP: rs1799929
rs1799929
0.776 0.240 8 18400484 synonymous variant C/T snv 0.36 0.36
CUI: C0085669
Disease: Acute leukemia
Acute leukemia
0.010 1.000 1 2019 2019
dbSNP: rs1799929
rs1799929
0.776 0.240 8 18400484 synonymous variant C/T snv 0.36 0.36
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs1799929
rs1799929
0.776 0.240 8 18400484 synonymous variant C/T snv 0.36 0.36
CUI: C0021364
Disease: Male infertility
Male infertility
0.010 1.000 1 2018 2018
dbSNP: rs1799929
rs1799929
0.776 0.240 8 18400484 synonymous variant C/T snv 0.36 0.36
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs1799929
rs1799929
0.776 0.240 8 18400484 synonymous variant C/T snv 0.36 0.36
CUI: C3203670
Disease: NAT2 polymorphism
NAT2 polymorphism
0.010 1.000 1 2012 2012
dbSNP: rs1799929
rs1799929
0.776 0.240 8 18400484 synonymous variant C/T snv 0.36 0.36
Slow acetylator due to N-acetyltransferase enzyme variant
0.010 1.000 1 2006 2006
dbSNP: rs1799929
rs1799929
0.776 0.240 8 18400484 synonymous variant C/T snv 0.36 0.36
CUI: C0029172
Disease: Oral Submucous Fibrosis
Oral Submucous Fibrosis
0.010 1.000 1 2012 2012
dbSNP: rs1799929
rs1799929
0.776 0.240 8 18400484 synonymous variant C/T snv 0.36 0.36
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.010 1.000 1 2017 2017
dbSNP: rs1799929
rs1799929
0.776 0.240 8 18400484 synonymous variant C/T snv 0.36 0.36
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 1997 1997