BRD2, bromodomain containing 2, 6046

N. diseases: 303; N. variants: 20
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: rs1049526
rs1049526
0.925 0.040 6 32981027 3 prime UTR variant C/T snv 0.93
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1049526
rs1049526
0.925 0.040 6 32981027 3 prime UTR variant C/T snv 0.93
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1049526
rs1049526
0.925 0.040 6 32981027 3 prime UTR variant C/T snv 0.93
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
Digestive System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs17840186
rs17840186
1.000 0.080 6 32970422 non coding transcript exon variant G/A snv 6.6E-02
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs3918149
rs3918149
1.000 0.040 6 32968596 5 prime UTR variant G/A snv 0.11
CUI: C0270853
Disease: Juvenile Myoclonic Epilepsy
Juvenile Myoclonic Epilepsy
Nervous System Diseases 0.040 0.750 4 2007 2019
dbSNP: rs1376873864
rs1376873864
0.925 0.080 6 32976646 missense variant G/A snv 4.1E-06
CUI: C0025322
Disease: Premature Menopause
Premature Menopause
Female Urogenital Diseases and Pregnancy Complications 0.030 0.667 3 2006 2010
dbSNP: rs1376873864
rs1376873864
0.925 0.080 6 32976646 missense variant G/A snv 4.1E-06
CUI: C0085215
Disease: Ovarian Failure, Premature
Ovarian Failure, Premature
Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.030 0.667 3 2006 2010
dbSNP: rs184752888
rs184752888
0.882 0.120 6 32977847 missense variant G/A snv
CUI: C0085083
Disease: Ovarian Hyperstimulation Syndrome
Ovarian Hyperstimulation Syndrome
Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.020 0.500 2 2004 2009
dbSNP: rs184752888
rs184752888
0.882 0.120 6 32977847 missense variant G/A snv
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.020 1.000 2 2011 2013
dbSNP: rs184752888
rs184752888
0.882 0.120 6 32977847 missense variant G/A snv
CUI: C0021364
Disease: Male infertility
Male infertility
Male Urogenital Diseases 0.020 0.500 2 2011 2015
dbSNP: rs757975291
rs757975291
0.851 0.120 6 32976868 missense variant G/A snv 4.1E-06 7.0E-06
CUI: C0085215
Disease: Ovarian Failure, Premature
Ovarian Failure, Premature
Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.020 1.000 2 2004 2007
dbSNP: rs757975291
rs757975291
0.851 0.120 6 32976868 missense variant G/A snv 4.1E-06 7.0E-06
CUI: C0025322
Disease: Premature Menopause
Premature Menopause
Female Urogenital Diseases and Pregnancy Complications 0.020 1.000 2 2004 2007
dbSNP: rs1260256848
rs1260256848
6 32976634 missense variant G/T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
Neoplasms 0.010 < 0.001 1 2006 2006
dbSNP: rs1260256848
rs1260256848
6 32976634 missense variant G/T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
Neoplasms 0.010 < 0.001 1 2006 2006
dbSNP: rs12822
rs12822
1.000 0.080 6 32977925 stop gained G/A;T snv 1.5E-05
CUI: C0001080
Disease: Achondroplasia
Achondroplasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.010 1.000 1 2007 2007
dbSNP: rs1397150560
rs1397150560
1.000 0.080 6 32978186 missense variant A/G snv 4.1E-06
CUI: C0001080
Disease: Achondroplasia
Achondroplasia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.010 1.000 1 2001 2001
dbSNP: rs1440086679
rs1440086679
0.925 0.120 6 32979854 missense variant C/T snv 4.1E-06
CUI: C0085083
Disease: Ovarian Hyperstimulation Syndrome
Ovarian Hyperstimulation Syndrome
Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs1440086679
rs1440086679
0.925 0.120 6 32979854 missense variant C/T snv 4.1E-06
CUI: C0232939
Disease: Primary physiologic amenorrhea
Primary physiologic amenorrhea
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2010 2010
dbSNP: rs150794546
rs150794546
1.000 0.040 6 32976655 missense variant G/A snv 4.1E-06 7.0E-06
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
Endocrine System Diseases 0.010 < 0.001 1 2008 2008
dbSNP: rs184752888
rs184752888
0.882 0.120 6 32977847 missense variant G/A snv
CUI: C0085215
Disease: Ovarian Failure, Premature
Ovarian Failure, Premature
Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs199590043
rs199590043
1.000 0.080 6 32974624 synonymous variant G/C;T snv 1.6E-05; 8.0E-06
Follicle stimulating hormone deficiency
Nervous System Diseases; Endocrine System Diseases 0.010 1.000 1 2002 2002
dbSNP: rs201781653
rs201781653
0.925 0.080 6 32977805 missense variant C/A;T snv 4.1E-06; 1.6E-05
CUI: C0242343
Disease: Panhypopituitarism
Panhypopituitarism
Nervous System Diseases; Endocrine System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs201781653
rs201781653
0.925 0.080 6 32977805 missense variant C/A;T snv 4.1E-06; 1.6E-05
Adrenocorticotropic hormone (ACTH) deficiency (disorder)
Endocrine System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs748209924
rs748209924
1.000 0.040 6 32974462 missense variant G/C;T snv 4.0E-06; 4.0E-06
Hypogonadism, Isolated Hypogonadotropic
Endocrine System Diseases 0.010 1.000 1 2001 2001
dbSNP: rs757975291
rs757975291
0.851 0.120 6 32976868 missense variant G/A snv 4.1E-06 7.0E-06
CUI: C0232940
Disease: Secondary physiologic amenorrhea
Secondary physiologic amenorrhea
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2004 2004