Gene: FAM3C ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7776725
rs7776725
FAM3C
4 1.000 0.080 7 121393067 intron variant T/C snv 0.28 0.700 1.000 2 2009 2014
dbSNP: rs917727
rs917727
FAM3C
3 7 121378525 intron variant C/A;T snv 0.33 0.700 1.000 2 2012 2017
dbSNP: rs917726
rs917726
FAM3C
2 7 121378803 intron variant A/T snv 0.31 0.700 1.000 1 2018 2018