rs121913529, KRAS

N. diseases: 135
Source: BEFREE ×
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Childhood Acute Monoblastic Leukemia
CUI: C0279645
Disease: Childhood Acute Monoblastic Leukemia
5 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2014 2014
Childhood Angiosarcoma
CUI: C0279988
Disease: Childhood Angiosarcoma
1 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2016 2016
Childhood Embryonal Rhabdomyosarcoma
CUI: C0279612
Disease: Childhood Embryonal Rhabdomyosarcoma
7 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2018 2018
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1 2007 2007
Childhood Liposarcoma
CUI: C0279984
Disease: Childhood Liposarcoma
6 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2015 2015
Childhood Lymphoma
CUI: C1332979
Disease: Childhood Lymphoma
66 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2008 2008
Childhood Pilocytic Astrocytoma
CUI: C1332995
Disease: Childhood Pilocytic Astrocytoma
10 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2007 2007
Chronic Lymphocytic Leukemia
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
125 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 1997 1997
Chronic myeloproliferative disorder
CUI: C1292778
Disease: Chronic myeloproliferative disorder
44 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2017 2017
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2018 2018
Colonic Neoplasms
CUI: C0009375
Disease: Colonic Neoplasms
41 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2016 2016
Cystadenocarcinoma, Serous
CUI: C0206701
Disease: Cystadenocarcinoma, Serous
1 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2010 2010
Desmoplastic
CUI: C1511789
Disease: Desmoplastic
4 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2013 2013
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
109 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 1997 1997
Disseminated Malignant Neoplasm
CUI: C0346957
Disease: Disseminated Malignant Neoplasm
4 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2016 2016
Embryonal Rhabdomyosarcoma
CUI: C0206656
Disease: Embryonal Rhabdomyosarcoma
8 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2018 2018
Gestational Trophoblastic Neoplasms
CUI: C1135868
Disease: Gestational Trophoblastic Neoplasms
7 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2004 2004
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
157 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1 2007 2007
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
160 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1 2007 2007
granulosa cell tumor
CUI: C0018206
Disease: granulosa cell tumor
5 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2010 2010
Hemangiosarcoma
CUI: C0018923
Disease: Hemangiosarcoma
5 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2016 2016
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
269 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2018 2018
Hurthle Cell Tumor
CUI: C0949541
Disease: Hurthle Cell Tumor
9 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2013 2013
Intraductal papillary mucinous neoplasm
CUI: C3160815
Disease: Intraductal papillary mucinous neoplasm
2 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2016 2016
Juberg-Marsidi syndrome
CUI: C0796003
Disease: Juberg-Marsidi syndrome
4 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2019 2019