Source: CLINVAR

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: rs369160589
rs369160589
0.742 0.400 16 5082676 splice region variant A/G snv 1.0E-04 1.3E-04
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery
0.700 0
dbSNP: rs369160589
rs369160589
0.742 0.400 16 5082676 splice region variant A/G snv 1.0E-04 1.3E-04
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment
0.700 0
dbSNP: rs369160589
rs369160589
0.742 0.400 16 5082676 splice region variant A/G snv 1.0E-04 1.3E-04
CUI: C0039231
Disease: Tachycardia
Tachycardia
0.700 0
dbSNP: rs369160589
rs369160589
0.742 0.400 16 5082676 splice region variant A/G snv 1.0E-04 1.3E-04
CUI: C4281993
Disease: Neonatal respiratory distress
Neonatal respiratory distress
0.700 0
dbSNP: rs369160589
rs369160589
0.742 0.400 16 5082676 splice region variant A/G snv 1.0E-04 1.3E-04
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs369160589
rs369160589
0.742 0.400 16 5082676 splice region variant A/G snv 1.0E-04 1.3E-04
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia
0.700 0
dbSNP: rs369160589
rs369160589
0.742 0.400 16 5082676 splice region variant A/G snv 1.0E-04 1.3E-04
CUI: C0262655
Disease: Recurrent urinary tract infection
Recurrent urinary tract infection
0.700 0
dbSNP: rs369160589
rs369160589
0.742 0.400 16 5082676 splice region variant A/G snv 1.0E-04 1.3E-04
Small for gestational age (disorder)
0.700 0
dbSNP: rs369160589
rs369160589
0.742 0.400 16 5082676 splice region variant A/G snv 1.0E-04 1.3E-04
CUI: C0342546
Disease: Premature adrenarche
Premature adrenarche
0.700 0
dbSNP: rs369160589
rs369160589
0.742 0.400 16 5082676 splice region variant A/G snv 1.0E-04 1.3E-04
Congenital Disorders of Glycosylation
0.700 0