Gene: FNDC3B ×
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: rs9647379
rs9647379
FNDC3B
2 3 172067378 intron variant G/C snv 0.32 0.700 1.000 2 2018 2019
dbSNP: rs4894803
rs4894803
FNDC3B
1 3 172082466 intron variant A/G snv 0.33 0.700 1.000 1 2019 2019