rs1076562, DRD2

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.
OROFACIAL CLEFT 1
CUI: C1861537
Disease: OROFACIAL CLEFT 1
11 0.925 0.120 11 113425286 intron variant A/G snv 0.65 0.010 1.000 1 2011 2011
OTOFACIOCERVICAL SYNDROME 1
CUI: C3714941
Disease: OTOFACIOCERVICAL SYNDROME 1
10 0.925 0.120 11 113425286 intron variant A/G snv 0.65 0.010 1.000 1 2011 2011