rs1555031372, DPF2

N. diseases: 3
Source: CLINVAR ×
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.
COFFIN-SIRIS SYNDROME 7
CUI: C4747954
Disease: COFFIN-SIRIS SYNDROME 7
5 0.925 0.280 11 65345981 missense variant G/T snv 0.800 1.000 0 2018 2018
MENTAL RETARDATION, AUTOSOMAL DOMINANT 12
CUI: C3281201
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 12
61 0.925 0.280 11 65345981 missense variant G/T snv 0.700 1.000 1 2018 2018
Poor school performance
CUI: C1843367
Disease: Poor school performance
411 0.925 0.280 11 65345981 missense variant G/T snv 0.700 1.000 1 2018 2018