Promoter region
SNP position
SNP ID
Gene
Disease
Type
P-value
Source
chr20:34359896-34538292
chr20:34383634
rs11906854
PHF20
Migraine - clinic-based
intron
7e-06
GWASdb
chr20:34359896-34538292
chr20:34384646
rs17430100
PHF20
Protein C levels
intron
3.92e-45
GWASdb
chr20:34359896-34538292
chr20:34390527
rs6060612
PHF20
Common traits (Other)
intron
6.31e-10
GWASdb
chr20:34359896-34538292
chr20:34429931
rs17345771
PHF20
Protein C levels
intron
5.28e-45
GWASdb
chr20:34359896-34538292
chr20:34440380
rs2425168
PHF20
Protein C levels
intron
5.87e-45
GWASdb
chr20:34359896-34538292
chr20:34445142
rs2425173
PHF20
Protein C levels
intron
2.72e-08
GWASdb
chr20:34359896-34538292
chr20:34445375
rs2425174
PHF20
Protein C levels
intron
6.16e-45
GWASdb
chr20:34359896-34538292
chr20:34448810
rs2064511
PHF20
Protein C levels
intron
2.75e-08
GWASdb
chr20:34359896-34538292
chr20:34458599
rs6060649
PHF20
Protein C levels
intron
9.56e-45
GWASdb
chr20:34359896-34538292
chr20:34460479
rs6058339
PHF20
Melanoma
intron
1.69e-07
GWASdb
chr20:34359896-34538292
chr20:34470012
rs6060658
PHF20
Protein C levels
intron
3.03e-44
GWASdb
chr20:34359896-34538292
chr20:34489565
rs7267005
PHF20
Narcolepsy
intron
6.1e-32
GWASdb
chr20:34359896-34538292
chr20:34509678
rs6060684
PHF20
Protein C levels
intron
3.62e-44
GWASdb
chr20:34359896-34538292
chr20:34513655
rs6121089
PHF20
Protein C levels
intron
3.66e-44
GWASdb
chr20:34359896-34538292
chr20:34515490
rs6058368
PHF20
Protein C levels
intron
3.67e-44
GWASdb
chr20:34359896-34538292
chr20:34517135
rs6060690
PHF20
Protein C levels
intron
6.84e-45
GWASdb
chr20:34359896-34538292
chr20:34529734
rs6060702
PHF20
Multiple complex diseases
intron
0.000353
GWASdb