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: rs797045282
rs797045282
1.000 0.280 6 157206545 stop gained C/T snv
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0.700 1.000 20 1984 2017
dbSNP: rs797045282
rs797045282
1.000 0.280 6 157206545 stop gained C/T snv
MENTAL RETARDATION, AUTOSOMAL DOMINANT 12
0.700 0