List of variants in gene TRIO reported as uncertain significance by New York Genome Center

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_007118.4(TRIO):c.9277C>T (p.Leu3093Phe)	rs145985294	0.00039
NM_007118.4(TRIO):c.7922A>C (p.Lys2641Thr)	rs200539540	0.00016
NM_007118.4(TRIO):c.410C>T (p.Ser137Phe)	rs961247277	0.00002
NM_007118.4(TRIO):c.53C>G (p.Ala18Gly)	rs1429556466	0.00001
NM_007118.4(TRIO):c.6725C>T (p.Thr2242Met)	rs55916212	0.00001
NM_007118.4(TRIO):c.7250G>A (p.Ser2417Asn)	rs927883781	0.00001
NM_007118.4(TRIO):c.8686C>A (p.Leu2896Met)	rs1422150009	0.00001
NM_007118.4(TRIO):c.2046+6G>T	rs1741451308
NM_007118.4(TRIO):c.4978C>A (p.Leu1660Met)	rs2152389359
NM_007118.4(TRIO):c.5056C>G (p.Leu1686Val)	rs749494831
NM_007118.4(TRIO):c.7001G>C (p.Ser2334Thr)	rs375274497
NM_007118.4(TRIO):c.8019+6T>G	rs2126677662
NM_007118.4(TRIO):c.8383T>C (p.Phe2795Leu)	rs944775553

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