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: rs7623687
rs7623687
RHOA ; TCTA
1.000 0.040 3 49411133 intron variant A/C;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 3 2017 2018
dbSNP: rs1057519951
rs1057519951
RHOA
0.882 0.080 3 49375472 missense variant C/G;T snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs1057519951
rs1057519951
RHOA
0.882 0.080 3 49375472 missense variant C/G;T snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs1057519951
rs1057519951
RHOA
0.882 0.080 3 49375472 missense variant C/G;T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 1.000 1 2016 2016
dbSNP: rs1057519951
rs1057519951
RHOA
0.882 0.080 3 49375472 missense variant C/G;T snv
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
Squamous cell carcinoma of the head and neck 		0.700 1.000 1 2016 2016
dbSNP: rs1057519952
rs1057519952
RHOA
0.882 0.160 3 49375577 missense variant G/A snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs1057519952
rs1057519952
RHOA
0.882 0.160 3 49375577 missense variant G/A snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs1057519952
rs1057519952
RHOA
0.882 0.160 3 49375577 missense variant G/A snv
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial 		0.700 1.000 1 2016 2016
dbSNP: rs1057519952
rs1057519952
RHOA
0.882 0.160 3 49375577 missense variant G/A snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs1057519952
rs1057519952
RHOA
0.882 0.160 3 49375577 missense variant G/A snv
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs1057519953
rs1057519953
RHOA
0.807 0.200 3 49375576 missense variant C/A;T snv
CUI: C0152018
Disease: Esophageal carcinoma
Esophageal carcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs1057519953
rs1057519953
RHOA
0.807 0.200 3 49375576 missense variant C/A;T snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs1057519953
rs1057519953
RHOA
0.807 0.200 3 49375576 missense variant C/A;T snv
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 1 2016 2016
dbSNP: rs1057519953
rs1057519953
RHOA
0.807 0.200 3 49375576 missense variant C/A;T snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs1057519953
rs1057519953
RHOA
0.807 0.200 3 49375576 missense variant C/A;T snv
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial 		0.700 1.000 1 2016 2016
dbSNP: rs1057519954
rs1057519954
RHOA
0.882 0.160 3 49375465 missense variant T/A;C;G snv
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
Lymphoma, Non-Hodgkin, Familial 		0.700 1.000 1 2016 2016
dbSNP: rs1057519954
rs1057519954
RHOA
0.882 0.160 3 49375465 missense variant T/A;C;G snv
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		0.700 1.000 1 2016 2016
dbSNP: rs1057519954
rs1057519954
RHOA
0.882 0.160 3 49375465 missense variant T/A;C;G snv
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
Squamous cell carcinoma of the head and neck 		0.700 1.000 1 2016 2016
dbSNP: rs11716948
rs11716948
RHOA
3 49394470 intron variant C/T snv 0.19
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs1987628
rs1987628
RHOA
3 49361826 intron variant G/A snv 0.28
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs6784820
rs6784820
RHOA ; TCTA
1.000 0.040 3 49413431 intron variant A/G snv 0.40
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2008 2008
dbSNP: rs7623659
rs7623659
RHOA
3 49377358 intron variant C/T snv 0.30
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs7648841
rs7648841
RHOA
1.000 0.040 3 49379392 intron variant G/A snv 0.29
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2007 2007
dbSNP: rs1057519953
rs1057519953
RHOA
0.807 0.200 3 49375576 missense variant C/A;T snv
CUI: C0278879
Disease: Childhood Burkitt Lymphoma
Childhood Burkitt Lymphoma 		0.010 1.000 1 2014 2014
dbSNP: rs1057519953
rs1057519953
RHOA
0.807 0.200 3 49375576 missense variant C/A;T snv
CUI: C0278764
Disease: Adult Burkitt Lymphoma
Adult Burkitt Lymphoma 		0.010 1.000 1 2014 2014