BANP, BTG3 associated nuclear protein, 54971

N. diseases: 27; N. variants: 4
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: rs4843747
rs4843747
16 87957445 intron variant A/C snv 0.83
CUI: C1629609
Disease: Age at menopause
Age at menopause
0.800 1.000 1 2009 2009
dbSNP: rs12923739
rs12923739
16 88040229 intron variant C/A;G snv
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs6540125
rs6540125
16 87960283 intron variant T/G snv 0.68
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2018 2018
dbSNP: rs9927732
rs9927732
0.925 0.040 16 88043118 intron variant C/A;G;T snv
Necrotizing enterocolitis in fetus OR newborn
Digestive System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs9927732
rs9927732
0.925 0.040 16 88043118 intron variant C/A;G;T snv
CUI: C0151526
Disease: Premature Birth
Premature Birth
Female Urogenital Diseases and Pregnancy Complications 0.700 1.000 1 2018 2018
dbSNP: rs9927732
rs9927732
0.925 0.040 16 88043118 intron variant C/A;G;T snv
CUI: C0520459
Disease: Necrotizing Enterocolitis
Necrotizing Enterocolitis
Digestive System Diseases 0.700 1.000 1 2018 2018