Source: CLINVAR

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: rs371769427
rs371769427
0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
MYELODYSPLASTIC SYNDROME
0.850 1.000 2 2013 2019
dbSNP: rs371769427
rs371769427
0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.730 0.750 1 2016 2019
dbSNP: rs371769427
rs371769427
0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 4 2011 2016
dbSNP: rs371246226
rs371246226
0.827 0.160 21 43094667 missense variant T/C;G snv 2.4E-05; 2.4E-05
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 2 2011 2012
dbSNP: rs371769427
rs371769427
0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06
Transitional cell carcinoma of bladder
0.700 1.000 1 2016 2016
dbSNP: rs371769427
rs371769427
0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06
CUI: C0281361
Disease: Adenocarcinoma of pancreas
Adenocarcinoma of pancreas
0.700 1.000 1 2016 2016
dbSNP: rs371769427
rs371769427
0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06
CUI: C0280630
Disease: Uterine Carcinosarcoma
Uterine Carcinosarcoma
0.700 1.000 1 2016 2016
dbSNP: rs371769427
rs371769427
0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06
CUI: C0153574
Disease: Malignant Uterine Corpus Neoplasm
Malignant Uterine Corpus Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs371769427
rs371769427
0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06
CUI: C0007873
Disease: Uterine Cervical Neoplasm
Uterine Cervical Neoplasm
0.700 1.000 1 2016 2016
dbSNP: rs371769427
rs371769427
0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06
Squamous cell carcinoma of the head and neck
0.700 1.000 1 2016 2016