PRDM2, PR/SET domain 2, 7799

N. diseases: 115; N. variants: 8
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: rs2697963
rs2697963
1 13824245 3 prime UTR variant G/A;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs61775135
rs61775135
1.000 0.080 1 13821912 intron variant C/A snv 0.11
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm
Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1203633
rs1203633
1.000 0.040 1 13760080 intron variant C/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs1350533716
rs1350533716
0.925 0.080 1 13780080 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2004 2004
dbSNP: rs1350533716
rs1350533716
0.925 0.080 1 13780080 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2004 2004
dbSNP: rs17350795
rs17350795
1.000 0.080 1 13779144 missense variant G/A snv 2.8E-02 1.5E-02
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2015 2015
dbSNP: rs2744687
rs2744687
1.000 0.040 1 13812318 intron variant T/G snv 0.88
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs2744690
rs2744690
1.000 0.040 1 13811306 intron variant A/C snv 0.87
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs761320613
rs761320613
0.925 0.080 1 13780842 missense variant C/T snv 4.0E-06
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2004 2004
dbSNP: rs761320613
rs761320613
0.925 0.080 1 13780842 missense variant C/T snv 4.0E-06
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2004 2004