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: rs1056892
rs1056892
0.882 0.160 21 36146408 missense variant G/A snv 0.37 0.39
CUI: C0278704
Disease: Malignant Childhood Neoplasm
Malignant Childhood Neoplasm
0.020 1.000 2 2008 2012
dbSNP: rs1056892
rs1056892
0.882 0.160 21 36146408 missense variant G/A snv 0.37 0.39
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.010 1.000 1 2008 2008
dbSNP: rs1056892
rs1056892
0.882 0.160 21 36146408 missense variant G/A snv 0.37 0.39
Carcinoma of urinary bladder, invasive
0.010 1.000 1 2018 2018
dbSNP: rs1056892
rs1056892
0.882 0.160 21 36146408 missense variant G/A snv 0.37 0.39
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies
0.010 1.000 1 2012 2012
dbSNP: rs1056892
rs1056892
0.882 0.160 21 36146408 missense variant G/A snv 0.37 0.39
CUI: C0018802
Disease: Congestive heart failure
Congestive heart failure
0.010 1.000 1 2008 2008
dbSNP: rs1056892
rs1056892
0.882 0.160 21 36146408 missense variant G/A snv 0.37 0.39
CUI: C0521158
Disease: Recurrent tumor
Recurrent tumor
0.010 1.000 1 2018 2018