rs6060373, UQCC1

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Body Height
CUI: C0005890
Disease: Body Height
3972 0.925 0.200 20 35326405 intron variant A/G snv 0.49 0.700 1.000 2 2008 2019
Height
CUI: C0489786
Disease: Height
517 0.925 0.200 20 35326405 intron variant A/G snv 0.49 0.700 1.000 1 2008 2008
Congenital Dysplasia Of The Hip
CUI: C4551649
Disease: Congenital Dysplasia Of The Hip
27 0.925 0.200 20 35326405 intron variant A/G snv 0.49 0.010 1.000 1 2015 2015
Testicular Germ Cell Tumor
CUI: C1336708
Disease: Testicular Germ Cell Tumor
93 0.925 0.200 20 35326405 intron variant A/G snv 0.49 0.010 1.000 1 2011 2011