Source: UNIPROT

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: rs1215280530
rs1215280530
CTCF
16 67616822 missense variant A/G snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms 		0.700 0
dbSNP: rs35766612
rs35766612
TGFBR2
3 30672342 missense variant G/A;T snv 1.0E-03; 3.5E-04
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms 		0.700 0