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: rs12461110
rs12461110 		19 55809297 missense variant G/A snv 0.32 0.26
CUI: C1629609
Disease: Age at menopause
Age at menopause 		0.800 1.000 3 2012 2015
dbSNP: rs12461110
rs12461110 		19 55809297 missense variant G/A snv 0.32 0.26
CUI: C0005612
Disease: Birth Weight
Birth Weight 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2019 2019
dbSNP: rs2547274
rs2547274 		19 55798862 intron variant G/C snv 6.5E-02
CUI: C1629609
Disease: Age at menopause
Age at menopause 		0.700 1.000 1 2015 2015
dbSNP: rs299163
rs299163 		19 55810048 missense variant C/A;T snv 0.96
CUI: C1629609
Disease: Age at menopause
Age at menopause 		0.700 1.000 1 2019 2019
dbSNP: rs1363758
rs1363758 		1.000 0.040 19 55818381 intron variant G/T snv 8.1E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 1.000 1 2010 2010