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: rs6672420
rs6672420
RUNX3 ; LOC105376878
0.827 0.120 1 24964519 missense variant A/T snv 0.56 0.50
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 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: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.020 0.500 2 2015 2017
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: 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