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: rs11217878
rs11217878
ARHGEF12
2 1.000 0.040 11 120469674 intron variant G/A snv 0.20 0.700 1.000 3 2015 2018
dbSNP: rs11217863
rs11217863
ARHGEF12
2 11 120422429 intron variant G/A snv 8.6E-02 0.700 1.000 2 2015 2018
dbSNP: rs12794618
rs12794618
ARHGEF12
1 11 120418990 intron variant T/C snv 0.21 0.700 1.000 2 2015 2017
dbSNP: rs10502235
rs10502235
ARHGEF12
1 11 120341714 intron variant A/G snv 0.19 0.700 1.000 1 2015 2015
dbSNP: rs10790381
rs10790381
ARHGEF12
1 11 120386786 intron variant A/G snv 0.20 0.700 1.000 1 2015 2015
dbSNP: rs10892565
rs10892565
ARHGEF12
1 11 120364851 intron variant T/C snv 0.21 0.700 1.000 1 2015 2015
dbSNP: rs10892569
rs10892569
ARHGEF12
1 11 120399540 intron variant A/G snv 0.19 0.700 1.000 1 2015 2015
dbSNP: rs10892575
rs10892575
ARHGEF12
1 11 120420428 intron variant C/G snv 0.20 0.700 1.000 1 2015 2015
dbSNP: rs11217843
rs11217843
ARHGEF12
1 11 120369228 intron variant A/G snv 0.20 0.700 1.000 1 2015 2015
dbSNP: rs11217857
rs11217857
ARHGEF12
1 11 120399461 intron variant A/G snv 0.21 0.700 1.000 1 2015 2015
dbSNP: rs11217866
rs11217866
ARHGEF12
1 11 120430095 intron variant T/A snv 0.20 0.700 1.000 1 2015 2015
dbSNP: rs11217874
rs11217874
ARHGEF12
1 11 120454839 intron variant G/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs11217875
rs11217875
ARHGEF12
1 11 120454850 intron variant C/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs11823264
rs11823264
ARHGEF12
1 11 120423295 intron variant G/A snv 0.20 0.700 1.000 1 2015 2015
dbSNP: rs11824032
rs11824032
ARHGEF12
1 11 120354080 intron variant G/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs12270397
rs12270397
ARHGEF12
1 11 120377633 intron variant C/T snv 0.21 0.700 1.000 1 2015 2015
dbSNP: rs12785387
rs12785387
ARHGEF12
1 11 120351278 intron variant C/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs12807097
rs12807097
ARHGEF12
1 11 120371639 intron variant G/A snv 0.19 0.700 1.000 1 2015 2015
dbSNP: rs17123861
rs17123861
ARHGEF12
1 11 120385628 intron variant T/C snv 0.21 0.700 1.000 1 2015 2015
dbSNP: rs1812974
rs1812974
ARHGEF12
1 11 120350359 intron variant C/T snv 0.21 0.700 1.000 1 2015 2015
dbSNP: rs199800298
rs199800298
ARHGEF12
1 11 120477875 intron variant G/- del 2.3E-03 0.700 1.000 1 2017 2017
dbSNP: rs2276035
rs2276035
ARHGEF12
1 11 120475651 intron variant G/A 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: rs4936518
rs4936518
ARHGEF12
1 11 120440489 intron variant A/T snv 0.21 0.700 1.000 1 2015 2015
dbSNP: rs4938802
rs4938802
ARHGEF12
1 11 120358280 intron variant A/G snv 0.19 0.700 1.000 1 2015 2015