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: rs2066992
rs2066992
0.807 0.200 7 22728630 non coding transcript exon variant G/T snv 9.4E-02
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2014 2014
dbSNP: rs2066992
rs2066992
0.807 0.200 7 22728630 non coding transcript exon variant G/T snv 9.4E-02
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs2066992
rs2066992
0.807 0.200 7 22728630 non coding transcript exon variant G/T snv 9.4E-02
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.010 1.000 1 2017 2017
dbSNP: rs2066992
rs2066992
0.807 0.200 7 22728630 non coding transcript exon variant G/T snv 9.4E-02
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs2066992
rs2066992
0.807 0.200 7 22728630 non coding transcript exon variant G/T snv 9.4E-02
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium
0.010 1.000 1 2019 2019
dbSNP: rs2066992
rs2066992
0.807 0.200 7 22728630 non coding transcript exon variant G/T snv 9.4E-02
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 1.000 1 2015 2015