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: rs10046
rs10046
CYP19A1 ; MIR4713HG
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.100 0.818 11 2008 2018
dbSNP: rs10046
rs10046
CYP19A1 ; MIR4713HG
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.100 0.818 11 2008 2018
dbSNP: rs10046
rs10046
CYP19A1 ; MIR4713HG
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43
CUI: C0014175
Disease: Endometriosis
Endometriosis 		0.030 0.667 3 2011 2016
dbSNP: rs10046
rs10046
CYP19A1 ; MIR4713HG
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.020 0.500 2 2008 2018
dbSNP: rs10046
rs10046
CYP19A1 ; MIR4713HG
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43
CUI: C0085215
Disease: Ovarian Failure, Premature
Ovarian Failure, Premature 		0.020 1.000 2 2011 2011
dbSNP: rs10046
rs10046
CYP19A1 ; MIR4713HG
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43
CUI: C0025322
Disease: Premature Menopause
Premature Menopause 		0.020 1.000 2 2011 2011
dbSNP: rs10046
rs10046
CYP19A1 ; MIR4713HG
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2010 2010
dbSNP: rs10046
rs10046
CYP19A1 ; MIR4713HG
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43
CUI: C4552766
Disease: Miscarriage
Miscarriage 		0.010 1.000 1 2009 2009
dbSNP: rs10046
rs10046
CYP19A1 ; MIR4713HG
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.010 1.000 1 2011 2011
dbSNP: rs10046
rs10046
CYP19A1 ; MIR4713HG
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43
CUI: C0085083
Disease: Ovarian Hyperstimulation Syndrome
Ovarian Hyperstimulation Syndrome 		0.010 < 0.001 1 2008 2008
dbSNP: rs10046
rs10046
CYP19A1 ; MIR4713HG
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43
CUI: C0007103
Disease: Malignant neoplasm of endometrium
Malignant neoplasm of endometrium 		0.010 1.000 1 2012 2012
dbSNP: rs10046
rs10046
CYP19A1 ; MIR4713HG
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.010 1.000 1 2012 2012
dbSNP: rs10046
rs10046
CYP19A1 ; MIR4713HG
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		0.010 1.000 1 2008 2008
dbSNP: rs10046
rs10046
CYP19A1 ; MIR4713HG
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2010 2010
dbSNP: rs10046
rs10046
CYP19A1 ; MIR4713HG
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.010 1.000 1 2014 2014
dbSNP: rs10046
rs10046
CYP19A1 ; MIR4713HG
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 < 0.001 1 2019 2019
dbSNP: rs10046
rs10046
CYP19A1 ; MIR4713HG
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43
CUI: C0600142
Disease: Hot flushes
Hot flushes 		0.010 1.000 1 2016 2016
dbSNP: rs10046
rs10046
CYP19A1 ; MIR4713HG
0.708 0.400 15 51210789 3 prime UTR variant G/A snv 0.45 0.43
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2015 2015