rs1303000329, DLC1

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.
Meningomyelocele
CUI: C0025312
Disease: Meningomyelocele
27 0.851 0.080 8 13110812 missense variant G/A;T snv 4.0E-06 0.700 0
Myelocele
CUI: C0086664
Disease: Myelocele
1 0.851 0.080 8 13110812 missense variant G/A;T snv 4.0E-06 0.700 0
NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO
30 0.851 0.080 8 13110812 missense variant G/A;T snv 4.0E-06 0.700 0
Spina Bifida Occulta
CUI: C0080174
Disease: Spina Bifida Occulta
6 0.851 0.080 8 13110812 missense variant G/A;T snv 4.0E-06 0.700 0