Source: BEFREE

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: rs6672420
rs6672420
RUNX3 ; LOC105376878
0.827 0.120 1 24964519 missense variant A/T snv 0.56 0.50
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.020 0.500 2 2015 2017
dbSNP: rs11249206
rs11249206
RUNX3 ; LOC105376878
0.851 0.160 1 24951491 intron variant C/T snv 0.48
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm 		0.010 1.000 1 2008 2008
dbSNP: rs11249206
rs11249206
RUNX3 ; LOC105376878
0.851 0.160 1 24951491 intron variant C/T snv 0.48
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder 		0.010 1.000 1 2008 2008
dbSNP: rs11249206
rs11249206
RUNX3 ; LOC105376878
0.851 0.160 1 24951491 intron variant C/T snv 0.48
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 < 0.001 1 2015 2015
dbSNP: rs11249206
rs11249206
RUNX3 ; LOC105376878
0.851 0.160 1 24951491 intron variant C/T snv 0.48
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
Malignant neoplasm of urinary bladder 		0.010 1.000 1 2008 2008
dbSNP: rs1395621
rs1395621
RUNX3 ; LOC105376878
1.000 0.040 1 24944081 intron variant T/C snv 0.64
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.010 1.000 1 2013 2013
dbSNP: rs2236851
rs2236851
RUNX3
1.000 0.040 1 24917063 intron variant C/T snv 0.12
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.010 1.000 1 2008 2008
dbSNP: rs2236852
rs2236852
RUNX3
1.000 0.080 1 24917276 intron variant A/G snv 0.45
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 < 0.001 1 2015 2015
dbSNP: rs6672420
rs6672420
RUNX3 ; LOC105376878
0.827 0.120 1 24964519 missense variant A/T snv 0.56 0.50
CUI: C0017154
Disease: Gastritis, Atrophic
Gastritis, Atrophic 		0.010 < 0.001 1 2009 2009
dbSNP: rs6672420
rs6672420
RUNX3 ; LOC105376878
0.827 0.120 1 24964519 missense variant A/T snv 0.56 0.50
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 < 0.001 1 2009 2009
dbSNP: rs6672420
rs6672420
RUNX3 ; LOC105376878
0.827 0.120 1 24964519 missense variant A/T snv 0.56 0.50
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma 		0.010 1.000 1 2019 2019
dbSNP: rs6672420
rs6672420
RUNX3 ; LOC105376878
0.827 0.120 1 24964519 missense variant A/T snv 0.56 0.50
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 < 0.001 1 2009 2009
dbSNP: rs760805
rs760805
RUNX3 ; LOC107984932
0.776 0.240 1 24925432 intron variant A/T snv 0.42
CUI: C0374997
Disease: Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site
Helicobacter pylori (H. pylori) infection in conditions classified elsewhere and of unspecified site 		0.010 1.000 1 2009 2009
dbSNP: rs760805
rs760805
RUNX3 ; LOC107984932
0.776 0.240 1 24925432 intron variant A/T snv 0.42
CUI: C0017154
Disease: Gastritis, Atrophic
Gastritis, Atrophic 		0.010 1.000 1 2009 2009
dbSNP: rs760805
rs760805
RUNX3 ; LOC107984932
0.776 0.240 1 24925432 intron variant A/T snv 0.42
CUI: C0004045
Disease: Asphyxia Neonatorum
Asphyxia Neonatorum 		0.010 1.000 1 2019 2019
dbSNP: rs760805
rs760805
RUNX3 ; LOC107984932
0.776 0.240 1 24925432 intron variant A/T snv 0.42
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
Malignant neoplasm of urinary bladder 		0.010 1.000 1 2008 2008
dbSNP: rs760805
rs760805
RUNX3 ; LOC107984932
0.776 0.240 1 24925432 intron variant A/T snv 0.42
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm 		0.010 1.000 1 2008 2008
dbSNP: rs760805
rs760805
RUNX3 ; LOC107984932
0.776 0.240 1 24925432 intron variant A/T snv 0.42
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder 		0.010 1.000 1 2008 2008
dbSNP: rs760805
rs760805
RUNX3 ; LOC107984932
0.776 0.240 1 24925432 intron variant A/T snv 0.42
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 < 0.001 1 2015 2015
dbSNP: rs906296
rs906296
RUNX3 ; LOC105376878
0.925 0.080 1 24938167 intron variant C/G snv 0.76
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2013 2013
dbSNP: rs906296
rs906296
RUNX3 ; LOC105376878
0.925 0.080 1 24938167 intron variant C/G snv 0.76
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs9438876
rs9438876
RUNX3
1.000 0.040 1 24914625 intron variant A/G snv 0.53
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.010 1.000 1 2013 2013