Gene: ARHGEF3 ×
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: rs1354034
rs1354034
ARHGEF3
4 3 56815721 intron variant T/C snv 0.49 0.800 1.000 4 2011 2019
dbSNP: rs12485738
rs12485738
ARHGEF3
1 3 56831748 intron variant A/G snv 0.63 0.800 1.000 3 2009 2012
dbSNP: rs11459029
rs11459029
ARHGEF3
1 3 56740187 intron variant -/A delins 0.700 1.000 1 2016 2016
dbSNP: rs13098914
rs13098914
ARHGEF3
1 3 56800771 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs17825630
rs17825630
ARHGEF3
2 3 56916027 intron variant G/A snv 0.12 0.700 1.000 1 2016 2016