rs770992098, NEB

N. diseases: 2
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.
Developmental Disabilities
CUI: C0008073
Disease: Developmental Disabilities
19 1.000 0.080 2 151724954 missense variant T/C snv 8.0E-06 7.0E-06 0.010 1.000 1 2019 2019
dowling-degos disease
CUI: C3714534
Disease: dowling-degos disease
7 1.000 0.080 2 151724954 missense variant T/C snv 8.0E-06 7.0E-06 0.010 1.000 1 2019 2019