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: rs1174612410
rs1174612410
SLC12A9
0.882 0.080 7 100860016 missense variant A/G snv 4.0E-06 7.0E-06
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 1.000 1 1999 1999
dbSNP: rs1174612410
rs1174612410
SLC12A9
0.882 0.080 7 100860016 missense variant A/G snv 4.0E-06 7.0E-06
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.010 1.000 1 1999 1999
dbSNP: rs1174612410
rs1174612410
SLC12A9
0.882 0.080 7 100860016 missense variant A/G snv 4.0E-06 7.0E-06
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.010 1.000 1 1999 1999
dbSNP: rs138106763
rs138106763
SLC12A9
1.000 0.040 7 100857102 missense variant A/G snv 7.2E-05 1.2E-04
CUI: C0025202
Disease: melanoma
melanoma 		0.010 1.000 1 1998 1998
dbSNP: rs138106763
rs138106763
SLC12A9
1.000 0.040 7 100857102 missense variant A/G snv 7.2E-05 1.2E-04
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.010 1.000 1 1998 1998
dbSNP: rs34012126
rs34012126
SLC12A9
7 100855831 frameshift variant G/- delins
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 1999 1999
dbSNP: rs747097215
rs747097215
SLC12A9
1.000 0.080 7 100856990 missense variant C/T snv 2.0E-05 2.1E-05
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 1996 1996
dbSNP: rs758448528
rs758448528
SLC12A9
7 100860024 missense variant G/T snv 4.0E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2013 2013
dbSNP: rs758448528
rs758448528
SLC12A9
7 100860024 missense variant G/T snv 4.0E-06
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2013 2013