Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11868708
rs11868708
Entrez Id: 6470;102466733
Gene Symbol: SHMT1;MIR6778
SHMT1;MIR6778
CUI: C0023452
Disease:
Childhood Acute Lymphoblastic Leukemia
0.010 GeneticVariation BEFREE The rs11868708 variant was not associated with risk/protection of childhood ALL (P>0.05). 26950450 2016