Source: CLINVAR

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: rs1057519725
rs1057519725
KRAS
0.851 0.320 12 25225627 missense variant G/A snv 7.0E-06
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		0.700 1.000 8 2005 2011
dbSNP: rs1057519725
rs1057519725
KRAS
0.851 0.320 12 25225627 missense variant G/A snv 7.0E-06
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm 		0.700 1.000 3 2009 2013