Gene: ARHGEF12 ×
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: rs4938807
rs4938807
ARHGEF12
1 11 120460992 intron variant C/A snv 0.21 0.700 1.000 1 2015 2015
dbSNP: rs58073046
rs58073046
ARHGEF12
2 1.000 0.040 11 120377784 intron variant A/G snv 8.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs7129944
rs7129944
ARHGEF12
1 11 120428998 intron variant T/C snv 0.20 0.700 1.000 1 2015 2015
dbSNP: rs2305013
rs2305013
ARHGEF12
3 11 120469351 missense variant A/G;T snv 6.2E-02 4.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs76693355
rs76693355
ARHGEF12
1 11 120421768 intron variant T/C snv 0.12 8.6E-02 0.700 1.000 1 2015 2015