Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs750893877
rs750893877
0.807 0.320 17 7674258 synonymous variant G/A snv 8.0E-06
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.030 1.000 3 2016 2017
dbSNP: rs750893877
rs750893877
0.807 0.320 17 7674258 synonymous variant G/A snv 8.0E-06
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs750893877
rs750893877
0.807 0.320 17 7674258 synonymous variant G/A snv 8.0E-06
CUI: C0206634
Disease: Liposarcoma, Myxoid
Liposarcoma, Myxoid
0.010 1.000 1 2016 2016
dbSNP: rs750893877
rs750893877
0.807 0.320 17 7674258 synonymous variant G/A snv 8.0E-06
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme
0.010 1.000 1 2016 2016
dbSNP: rs750893877
rs750893877
0.807 0.320 17 7674258 synonymous variant G/A snv 8.0E-06
CUI: C0238461
Disease: Anaplastic thyroid carcinoma
Anaplastic thyroid carcinoma
0.010 1.000 1 2017 2017
dbSNP: rs750893877
rs750893877
0.807 0.320 17 7674258 synonymous variant G/A snv 8.0E-06
ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE, X-LINKED
0.010 1.000 1 2019 2019
dbSNP: rs750893877
rs750893877
0.807 0.320 17 7674258 synonymous variant G/A snv 8.0E-06
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia
0.010 1.000 1 2017 2017