Gene: ARHGEF38 ×
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: rs11725523
rs11725523
ARHGEF38
2 4 105596709 intron variant G/A snv 4.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11726569
rs11726569
ARHGEF38 ; INTS12
2 4 105685451 intron variant A/G snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11727189
rs11727189
ARHGEF38 ; INTS12
4 4 105697983 intron variant G/T snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11728044
rs11728044
ARHGEF38 ; INTS12
2 4 105683629 intron variant G/C snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs11735213
rs11735213
ARHGEF38
2 4 105606351 intron variant T/G snv 6.2E-02 0.700 1.000 1 2010 2010
dbSNP: rs12374256
rs12374256
ARHGEF38 ; INTS12
2 4 105696204 intron variant G/A snv 5.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs1374531
rs1374531
ARHGEF38
2 4 105602775 intron variant C/A snv 7.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs17035917
rs17035917
ARHGEF38
3 1.000 0.040 4 105599585 intron variant C/T snv 8.1E-02 0.700 1.000 1 2010 2010
dbSNP: rs17035960
rs17035960
ARHGEF38
2 4 105610689 intron variant C/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs17036052
rs17036052
ARHGEF38
2 4 105642222 intron variant C/T snv 3.6E-02 0.700 1.000 1 2010 2010
dbSNP: rs17036076
rs17036076
ARHGEF38
2 4 105654112 synonymous variant A/G snv 4.7E-02 5.0E-02 0.700 1.000 1 2010 2010
dbSNP: rs17036090
rs17036090
ARHGEF38
4 0.925 0.040 4 105672417 intron variant T/C snv 5.0E-02 0.700 1.000 1 2010 2010