Disease: NOONAN SYNDROME 7 ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121913369
rs121913369 		0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06
CUI: C3150970
Disease: NOONAN SYNDROME 7
NOONAN SYNDROME 7 		0.800 1.000 2 2009 2010
dbSNP: rs606231228
rs606231228 		0.925 0.160 7 140777013 missense variant C/A;G snv
CUI: C3150970
Disease: NOONAN SYNDROME 7
NOONAN SYNDROME 7 		0.800 1.000 1 2010 2010
dbSNP: rs387906660
rs387906660 		0.790 0.280 7 140801550 missense variant G/A;C;T snv
CUI: C3150970
Disease: NOONAN SYNDROME 7
NOONAN SYNDROME 7 		0.700 1.000 1 2009 2009
dbSNP: rs1562957000
rs1562957000 		1.000 7 140781621 missense variant T/C snv
CUI: C3150970
Disease: NOONAN SYNDROME 7
NOONAN SYNDROME 7 		0.700 0
dbSNP: rs180177042
rs180177042 		0.807 0.280 7 140749365 missense variant A/C;T snv
CUI: C3150970
Disease: NOONAN SYNDROME 7
NOONAN SYNDROME 7 		0.700 0
dbSNP: rs387906661
rs387906661 		0.807 0.280 7 140801551 missense variant T/G snv
CUI: C3150970
Disease: NOONAN SYNDROME 7
NOONAN SYNDROME 7 		0.700 0
dbSNP: rs397507466
rs397507466 		0.807 0.280 7 140801537 missense variant T/A;C;G snv 4.0E-06
CUI: C3150970
Disease: NOONAN SYNDROME 7
NOONAN SYNDROME 7 		0.700 0
dbSNP: rs397516895
rs397516895 		0.827 0.280 7 140753392 missense variant A/T snv
CUI: C3150970
Disease: NOONAN SYNDROME 7
NOONAN SYNDROME 7 		0.700 0