Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555727493
rs1555727493
KMT2B
CUI: C0234144
Disease: Dysgraphia
Dysgraphia 		TGGCGGCGGCGGCG 0.700 CausalMutation CLINVAR