Gene: ARHGAP24 ×
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: rs11732231
rs11732231
ARHGAP24
1 4 85762407 intron variant G/C;T snv 0.800 1.000 2 2012 2019
dbSNP: rs7692808
rs7692808
ARHGAP24
1 4 85719996 intron variant A/G;T snv 0.800 1.000 2 2010 2019
dbSNP: rs7660702
rs7660702
ARHGAP24
1 4 85730311 intron variant T/C snv 0.43 0.700 1.000 2 2010 2019
dbSNP: rs13105921
rs13105921
ARHGAP24
1 4 85778573 intron variant C/A snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs13111293
rs13111293
ARHGAP24
1 4 85761815 intron variant C/T snv 0.50 0.700 1.000 1 2019 2019
dbSNP: rs13137008
rs13137008
ARHGAP24
1 4 85753046 intron variant G/T snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs343849
rs343849
ARHGAP24
1 4 85741902 intron variant A/T snv 0.51 0.700 1.000 1 2018 2018