Gene: ARHGAP42 ×
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: rs633185
rs633185
ARHGAP42
10 0.925 0.080 11 100722807 intron variant G/A;C snv 0.700 1.000 8 2011 2018
dbSNP: rs604723
rs604723
ARHGAP42
9 1.000 0.040 11 100739815 intron variant T/C snv 0.78 0.700 1.000 2 2018 2019
dbSNP: rs6590811
rs6590811
ARHGAP42
4 11 100708153 intron variant C/T snv 0.53 0.700 1.000 2 2018 2018
dbSNP: rs10895025
rs10895025
ARHGAP42
1 11 100877772 intron variant T/C snv 0.63 0.700 1.000 1 2019 2019
dbSNP: rs486023
rs486023
ARHGAP42
2 11 100772406 intron variant G/A snv 0.25 0.700 1.000 1 2017 2017
dbSNP: rs6590816
rs6590816
ARHGAP42
4 11 100730902 intron variant G/A snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs670401
rs670401
ARHGAP42
3 11 100701679 intron variant A/G snv 0.76 0.700 1.000 1 2018 2018