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: rs365132
rs365132 		5 176951573 synonymous variant G/T snv 0.51 0.58
CUI: C1629609
Disease: Age at menopause
Age at menopause 		0.800 1.000 3 2009 2015
dbSNP: rs2456181
rs2456181 		1.000 5 177023836 intron variant C/G;T snv
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids 		Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs2456181
rs2456181 		1.000 5 177023836 intron variant C/G;T snv
CUI: C2242776
Disease: Plexiform leiomyoma
Plexiform leiomyoma 		0.700 1.000 1 2019 2019
dbSNP: rs353490
rs353490 		5 177006062 intron variant C/A;G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs365132
rs365132 		5 176951573 synonymous variant G/T snv 0.51 0.58
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2018 2018
dbSNP: rs58279426
rs58279426 		5 177021138 intron variant T/C snv 0.57
CUI: C1629609
Disease: Age at menopause
Age at menopause 		0.700 1.000 1 2019 2019
dbSNP: rs143282828
rs143282828 		1.000 0.080 5 176968697 missense variant A/G snv 7.3E-04 7.3E-04
CUI: C0346153
Disease: Breast Cancer, Familial
Breast Cancer, Familial 		Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2009 2009