SFTA2, surfactant associated 2, 389376

N. diseases: 25; N. variants: 13
Disease: Child Development Disorders, Pervasive ×
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: rs114115252
rs114115252 		1.000 0.040 6 30931418 3 prime UTR variant G/A;C;T snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs114838832
rs114838832 		1.000 0.040 6 30937536 intron variant A/G snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs3132581
rs3132581 		0.851 0.040 6 30945681 intron variant G/A snv 9.3E-02
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2013 2013