Gene: FFAR4 ×
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: rs11187537
rs11187537
FFAR4
1 10 93587048 intron variant G/C snv 0.29 0.700 1.000 2 2018 2019
dbSNP: rs12241416
rs12241416
FFAR4
1 10 93586671 intron variant G/A snv 0.29 0.700 1.000 1 2019 2019