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: rs1057518940
rs1057518940
0.925 0.040 19 38499718 missense variant G/A snv
CUI: C1850794
Disease: Proximal amyotrophy
Proximal amyotrophy
0.700 0
dbSNP: rs1057518940
rs1057518940
0.925 0.040 19 38499718 missense variant G/A snv
CUI: C0349588
Disease: Short stature
Short stature
0.700 0
dbSNP: rs1057518940
rs1057518940
0.925 0.040 19 38499718 missense variant G/A snv
CUI: C0332878
Disease: Congenital contracture
Congenital contracture
0.700 0
dbSNP: rs1057518940
rs1057518940
0.925 0.040 19 38499718 missense variant G/A snv
CUI: C1837658
Disease: Gross motor development delay
Gross motor development delay
0.700 0