Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1553924800
rs1553924800
1.000 4 84715350 missense variant G/A snv
MICROCEPHALY 18, PRIMARY, AUTOSOMAL DOMINANT
0.700 1.000 1 2016 2016
dbSNP: rs6847067
rs6847067
0.827 0.160 4 84811016 intron variant C/A snv 0.39
Malignant neoplasm of posterior wall of oropharynx
Neoplasms; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs6847067
rs6847067
0.827 0.160 4 84811016 intron variant C/A snv 0.39
malignant neoplasm of lateral wall of oropharynx
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs6847067
rs6847067
0.827 0.160 4 84811016 intron variant C/A snv 0.39
CUI: C0153382
Disease: Malignant neoplasm of oropharynx
Malignant neoplasm of oropharynx
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs6847067
rs6847067
0.827 0.160 4 84811016 intron variant C/A snv 0.39
CUI: C2349952
Disease: Oropharyngeal Carcinoma
Oropharyngeal Carcinoma
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs6847067
rs6847067
0.827 0.160 4 84811016 intron variant C/A snv 0.39
Primary malignant neoplasm of lateral wall of oropharynx
0.700 1.000 1 2016 2016