DHX37, DEAH-box helicase 37, 57647

N. diseases: 13; N. variants: 3
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: rs1060499737
rs1060499737 		12 124968903 missense variant G/T snv
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology 		0.700 0
dbSNP: rs1060499737
rs1060499737 		12 124968903 missense variant G/T snv
CUI: C4022738
Disease: Neurodevelopmental delay
Neurodevelopmental delay 		0.700 0
dbSNP: rs1060499737
rs1060499737 		12 124968903 missense variant G/T snv
CUI: C1843367
Disease: Poor school performance
Poor school performance 		0.700 0
dbSNP: rs779613772
rs779613772 		12 124967167 missense variant C/T snv 3.6E-05 5.6E-05
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology 		0.700 0
dbSNP: rs4606565
rs4606565 		1.000 0.040 12 124954003 splice region variant A/G snv 0.65 0.57
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.010 1.000 1 2006 2006
dbSNP: rs4606565
rs4606565 		1.000 0.040 12 124954003 splice region variant A/G snv 0.65 0.57
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2006 2006