rs4647269, MLH1

N. diseases: 2
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.
Oligospermia
CUI: C0028960
Disease: Oligospermia
72 0.925 0.040 3 37016100 intron variant C/T snv 0.35 0.020 1.000 2 2012 2019
Azoospermia
CUI: C0004509
Disease: Azoospermia
70 0.925 0.040 3 37016100 intron variant C/T snv 0.35 0.010 1.000 1 2012 2012