Source: BEFREE

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: rs12423791
rs12423791
IGF1
0.925 0.040 12 102465050 intron variant G/C snv 2.8E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2013 2013
dbSNP: rs12423791
rs12423791
IGF1
0.925 0.040 12 102465050 intron variant G/C snv 2.8E-02
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2016 2016
dbSNP: rs12423791
rs12423791
IGF1
0.925 0.040 12 102465050 intron variant G/C snv 2.8E-02
CUI: C0027092
Disease: Myopia
Myopia 		0.010 1.000 1 2012 2012
dbSNP: rs12423791
rs12423791
IGF1
0.925 0.040 12 102465050 intron variant G/C snv 2.8E-02
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2013 2013
dbSNP: rs12423791
rs12423791
IGF1
0.925 0.040 12 102465050 intron variant G/C snv 2.8E-02
CUI: C0271183
Disease: Severe myopia
Severe myopia 		0.010 < 0.001 1 2015 2015