Gene: ARHGAP15 ×
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: rs13428598
rs13428598
ARHGAP15
2 2 143492918 intron variant C/T snv 0.28 0.700 1.000 3 2018 2019
dbSNP: rs10191758
rs10191758
ARHGAP15
1 2 143505711 intron variant A/G snv 0.30 0.700 1.000 2 2017 2017
dbSNP: rs10189912
rs10189912
ARHGAP15
1 2 143405040 intron variant A/G snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs10200533
rs10200533
ARHGAP15
1 2 143425433 intron variant G/A snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs10204230
rs10204230
ARHGAP15
1 2 143512879 intron variant T/C snv 0.42 0.700 1.000 1 2018 2018
dbSNP: rs12465778
rs12465778
ARHGAP15
1 2 143497632 intron variant T/C snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs35825582
rs35825582
ARHGAP15
3 1.000 0.040 2 143491193 intron variant G/A snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs4233567
rs4233567
ARHGAP15
1 2 143514807 intron variant C/T snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs4273169
rs4273169
ARHGAP15
2 1.000 0.040 2 143473740 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs62172064
rs62172064
ARHGAP15
1 2 143397319 intron variant T/C snv 1.2E-02 0.700 1.000 1 2019 2019