Gene: ARVCF ×
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: rs2012714
rs2012714
ARVCF
1 22 19990124 intron variant C/T snv 0.34 0.700 1.000 2 2017 2018
dbSNP: rs1034565
rs1034565
ARVCF
1 22 19996688 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs117222687
rs117222687
ARVCF ; COMT
2 22 19968491 intron variant G/C snv 3.8E-02 4.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs2238787
rs2238787
ARVCF
1 22 19988883 intron variant G/A snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs758374
rs758374
ARVCF
2 22 19984029 intron variant T/C snv 0.27 0.700 1.000 1 2019 2019