rs180822335, COL13A1

N. diseases: 1
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.
Adverse effects, not elsewhere classified
CUI: C0869220
Disease: Adverse effects, not elsewhere classified
54 1.000 10 69950109 intron variant T/C snv 5.9E-03 0.700 1.000 1 2019 2019