PHF21A, PHD finger protein 21A, 51317

N. diseases: 50; N. variants: 16
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs16938437
rs16938437 		11 46031024 intron variant C/T snv 0.13
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.800 1.000 1 2010 2010
dbSNP: rs11038747
rs11038747 		11 46036689 intron variant T/C snv 1.8E-02
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11038755
rs11038755 		11 46057150 intron variant A/G snv 2.1E-02
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11038756
rs11038756 		11 46057507 intron variant T/C snv 2.6E-02
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11038764
rs11038764 		11 46098201 intron variant G/A snv 3.0E-02
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		0.700 1.000 1 2018 2018
dbSNP: rs12363382
rs12363382 		11 46091682 intron variant C/G snv 3.0E-02
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		0.700 1.000 1 2018 2018
dbSNP: rs140273453
rs140273453 		11 46007498 intron variant G/C snv 5.8E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs140876547
rs140876547 		11 45962517 intron variant G/A snv 3.2E-03
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs146033545
rs146033545 		11 46072184 intron variant T/A;G snv
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism 		Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1490088
rs1490088 		11 46086891 intron variant T/C snv 6.9E-02
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		0.700 1.000 1 2018 2018
dbSNP: rs16938437
rs16938437 		11 46031024 intron variant C/T snv 0.13
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs2932513
rs2932513 		11 46048627 intron variant G/A snv 0.75
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs2946005
rs2946005 		11 45979678 intron variant G/C snv 0.88
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4073513
rs4073513 		11 46049702 intron variant A/G snv 0.53
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs79686965
rs79686965 		11 45999358 intron variant A/G snv 2.0E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs79728014
rs79728014 		11 46040694 intron variant A/G snv 9.6E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs80171383
rs80171383 		11 46063126 intron variant G/A snv 9.3E-02
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2018 2018