Disease associated variation - ClinVar Allele ID Type Name RS#dbSNP Phenotype IDs Chromosome Start Stop Reference Alternate 171625 single nucleotide variant NM_001007525.4(NWD1):c.3668A>G (p.Asn1223Ser) 193920843 MedGen:C0376358,OMIM:176807,SNOMED CT:C0376358 19 16800094 16800094 A G 171625 single nucleotide variant NM_001007525.4(NWD1):c.3668A>G (p.Asn1223Ser) 193920843 MedGen:C0376358,OMIM:176807,SNOMED CT:C0376358 19 16910905 16910905 A G

Disease associated variation - GWASdb Chr Pos SNP ID(dbSNP 142) Ref Alt Ori SNP ID P-value Drug Name Drug Anno GWAS Trait HPO ID DO ID AA Type Trait or Drug 19 16899731 rs2547108 A G rs2547108 2.21E-05 Stroke HPOID:0001297 DOID:6713 G intron GWASdb_trait 19 16908639 rs73008597 C T rs73008597 0.0003 Prostate cancer HPOID:0012125 DOID:10283 C missense GWASdb_trait

Disease associated variation - OMIM Ensembl_gene_ID Approved Gene Symbol MIM Number ENSG00000188039.13 NWD1 616250