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: rs371582179
rs371582179
0.827 0.280 3 33014057 missense variant T/C snv 3.6E-05 6.3E-05
Gangliosidosis, Generalized GM1, Type 1 (disorder)
0.800 1.000 4 1991 2015
dbSNP: rs371582179
rs371582179
0.827 0.280 3 33014057 missense variant T/C snv 3.6E-05 6.3E-05
CUI: C0086652
Disease: Mucopolysaccharidosis type IVB
Mucopolysaccharidosis type IVB
0.700 1.000 4 1993 2015
dbSNP: rs371582179
rs371582179
0.827 0.280 3 33014057 missense variant T/C snv 3.6E-05 6.3E-05
Gangliosidosis, Generalized GM1, Type 2
0.700 1.000 4 1993 2015
dbSNP: rs371582179
rs371582179
0.827 0.280 3 33014057 missense variant T/C snv 3.6E-05 6.3E-05
Gangliosidosis, Generalized GM1, Type 3
0.700 1.000 4 1993 2015
dbSNP: rs371582179
rs371582179
0.827 0.280 3 33014057 missense variant T/C snv 3.6E-05 6.3E-05
Delayed speech and language development
0.700 0
dbSNP: rs371582179
rs371582179
0.827 0.280 3 33014057 missense variant T/C snv 3.6E-05 6.3E-05
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia
0.700 0
dbSNP: rs371582179
rs371582179
0.827 0.280 3 33014057 missense variant T/C snv 3.6E-05 6.3E-05
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability
0.700 0