rs1557178535, FLNA

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Chronic intestinal pseudo-obstruction
CUI: C0238062
Disease: Chronic intestinal pseudo-obstruction
10 0.851 0.120 X 154363633 intron variant A/T snv 0.700 0
Congenital idiopathic intestinal pseudoobstruction
CUI: C2746068
Disease: Congenital idiopathic intestinal pseudoobstruction
3 0.851 0.120 X 154363633 intron variant A/T snv 0.700 0
Periventricular Heterotopia, X-Linked
CUI: C1848213
Disease: Periventricular Heterotopia, X-Linked
38 0.851 0.120 X 154363633 intron variant A/T snv 0.700 0
Periventricular Nodular Heterotopia
CUI: C1868720
Disease: Periventricular Nodular Heterotopia
29 0.851 0.120 X 154363633 intron variant A/T snv 0.700 0