Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs112280096
rs112280096
BAHCC1 ; LOC100130370
17 81393609 upstream gene variant C/A snv 0.27
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2018 2018
dbSNP: rs113458760
rs113458760
BAHCC1
17 81396457 non coding transcript exon variant C/G;T snv 0.27
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019
dbSNP: rs1531554
rs1531554
BAHCC1
17 81406747 intron variant T/C snv 0.51
CUI: C0039494
Disease: Temporomandibular Joint Disorders
Temporomandibular Joint Disorders 		0.700 1.000 1 2017 2017
dbSNP: rs34386017
rs34386017
BAHCC1
17 81400162 intron variant G/A;C snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs35572189
rs35572189
BAHCC1 ; MIR3186
17 81451999 missense variant G/A;C snv 0.34
CUI: C0001925
Disease: Albuminuria
Albuminuria 		0.700 1.000 1 2018 2018
dbSNP: rs6565564
rs6565564
BAHCC1
17 81408117 intron variant G/C snv 0.96
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs77984483
rs77984483
BAHCC1
17 81435577 intron variant C/T snv 0.12
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs1701
rs1701
BAHCC1 ; MIR4740
17 81402198 non coding transcript exon variant C/A;G;T snv
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		0.010 1.000 1 2013 2013