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: rs1561498701
rs1561498701
SMN1 ; SMN2
1.000 0.080 5 70925150 frameshift variant -/GGATTCCG delins
CUI: C0393538
Disease: Muscular Atrophy, Spinal, Type II
Muscular Atrophy, Spinal, Type II 		0.700 1.000 1 2013 2013
dbSNP: rs1561498701
rs1561498701
SMN1 ; SMN2
1.000 0.080 5 70925150 frameshift variant -/GGATTCCG delins
CUI: C0234146
Disease: Absent reflex
Absent reflex 		0.700 1.000 1 2013 2013
dbSNP: rs1561498701
rs1561498701
SMN1 ; SMN2
1.000 0.080 5 70925150 frameshift variant -/GGATTCCG delins
CUI: C0239548
Disease: Fasciculation, Tongue
Fasciculation, Tongue 		0.700 1.000 1 2013 2013
dbSNP: rs1561498701
rs1561498701
SMN1 ; SMN2
1.000 0.080 5 70925150 frameshift variant -/GGATTCCG delins
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		0.700 1.000 1 2013 2013
dbSNP: rs1561498701
rs1561498701
SMN1 ; SMN2
1.000 0.080 5 70925150 frameshift variant -/GGATTCCG delins
CUI: C1839630
Disease: Severe muscular hypotonia
Severe muscular hypotonia 		0.700 1.000 1 2013 2013