Gene: PHF20 ×
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: rs17345771
rs17345771
PHF20
2 20 35842009 intron variant C/T snv 3.6E-02 0.700 1.000 1 2010 2010
dbSNP: rs17430100
rs17430100
PHF20
2 20 35796724 intron variant A/G snv 3.6E-02 0.700 1.000 1 2010 2010
dbSNP: rs2064511
rs2064511
PHF20
2 20 35860888 intron variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs2425168
rs2425168
PHF20
2 20 35852458 intron variant A/T snv 7.6E-02 0.700 1.000 1 2010 2010
dbSNP: rs2425173
rs2425173
PHF20
2 20 35857220 intron variant G/A snv 0.18 0.700 1.000 1 2010 2010
dbSNP: rs2425174
rs2425174
PHF20
2 20 35857453 intron variant C/A;G snv 0.700 1.000 1 2010 2010
dbSNP: rs6058368
rs6058368
PHF20
2 20 35927568 intron variant A/G snv 3.9E-02 0.700 1.000 1 2010 2010
dbSNP: rs6060649
rs6060649
PHF20
2 20 35870677 intron variant G/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs6060658
rs6060658
PHF20
2 20 35882090 intron variant T/G snv 7.6E-02 0.700 1.000 1 2010 2010
dbSNP: rs6060684
rs6060684
PHF20
2 20 35921756 intron variant T/G snv 7.8E-02 0.700 1.000 1 2010 2010
dbSNP: rs6060690
rs6060690
PHF20
2 20 35929213 intron variant T/C snv 7.8E-02 0.700 1.000 1 2010 2010
dbSNP: rs6121089
rs6121089
PHF20
2 20 35925733 intron variant G/A snv 9.5E-02 0.700 1.000 1 2010 2010