Source: ALL

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: rs397507444
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv
CUI: C0085183
Disease: Neoplasms, Second Primary
Neoplasms, Second Primary 		0.010 1.000 1 2005 2005
dbSNP: rs75873440
rs75873440
RET
0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05
CUI: C0085183
Disease: Neoplasms, Second Primary
Neoplasms, Second Primary 		0.010 1.000 1 2017 2017