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: rs1432155504
rs1432155504
GGT2
1.000 0.080 22 21225543 missense variant C/G snv
CUI: C0040137
Disease: Thyroid Nodule
Thyroid Nodule 		0.010 1.000 1 2006 2006
dbSNP: rs765862970
rs765862970
GGT2
0.925 0.080 22 21208817 synonymous variant A/G snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2011 2011
dbSNP: rs765862970
rs765862970
GGT2
0.925 0.080 22 21208817 synonymous variant A/G snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.010 1.000 1 2011 2011