Rare Genetic Intellectual Disability

Other 45 variants 32 genes

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Associated Genes (32)

ANKRD11 KMT2A KMT5B MED13L KMT2D CHD8 KIF7 SRCAP CREBBP GPT2 KMT2C RAI1 TLK2 KMT2B EP300 OFD1 PTCHD1 DDX3X KDM3B GNAO1 MTOR WAC TUBA1A ALG13 FOXP1 KDM5C LAMA2 MTHFR DNMT3A SETD5 ARID1B PHIP

Associated Variants (45)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS2544223937	ANKRD11	—	—	strong
RS2496842029	KMT2A	—	—	strong
RS2496189023	KMT5B	—	—	strong
RS2499831679	MED13L	—	—	strong
RS2499931368	MED13L	—	—	strong
RS2499943377	MED13L	—	—	strong
RS2120361642	KMT2D	—	—	strong
RS2501857970	CHD8	—	—	strong
RS2505426700	KIF7	—	—	strong
RS2474004099	SRCAP	—	—	strong
RS2151312423	CREBBP	—	—	strong
RS2548963125	GPT2	—	—	strong
RS2093221854	KMT2C	—	—	strong
RS2544237769	ANKRD11	—	—	strong
RS2543620405	RAI1	—	—	strong
RS2545717131	TLK2	—	—	strong
RS2513330269	KMT2B	—	—	strong
RS2145766541	EP300	—	—	strong
RS748643730	OFD1	—	—	strong
RS2518760163	PTCHD1	—	—	strong
RS2147350816	DDX3X	—	—	strong
RS1602135832	DDX3X	—	—	strong
RS2126998820	KDM3B	—	—	strong
RS1555039343	KMT2A	—	—	strong
RS587777057	GNAO1	—	—	strong
RS796052230	DDX3X	—	—	strong
RS797045027	ANKRD11	—	—	strong
RS863225264	MTOR	—	—	strong
RS878855327	ANKRD11	—	—	strong
RS886039477	ANKRD11	—	—	strong
RS886041614	WAC	—	—	strong
RS886041125	ANKRD11	—	—	strong
RS886041518	CREBBP	—	—	strong
RS1064793286	TUBA1A	—	—	strong
RS398122394	ALG13	—	—	strong
RS1559602356	FOXP1	—	—	strong
RS1602163752	KDM5C	—	—	strong
RS370181941	LAMA2	—	—	strong
RS1434449406	MTHFR	—	—	strong
RS1674465974	DNMT3A	—	—	strong
RS2545122691	FOXP1	—	—	strong
RS2472723327	SETD5	—	—	strong
RS2473598536	SETD5	—	—	strong
RS1794569741	ARID1B	—	—	strong
RS754764007	PHIP	—	—	strong