List of variants in gene KCNQ5 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_019842.4(KCNQ5):c.2366A>T (p.Glu789Val)	rs771383058	0.00002
NM_019842.4(KCNQ5):c.1304T>A (p.Ile435Asn)	rs761319100	0.00001
NM_019842.4(KCNQ5):c.1906G>C (p.Ala636Pro)	rs774223061	0.00001
NM_019842.4(KCNQ5):c.1217C>T (p.Thr406Ile)
NM_019842.4(KCNQ5):c.1221-4G>A
NM_019842.4(KCNQ5):c.1577+8A>T	rs2150503672
NM_019842.4(KCNQ5):c.1772C>T (p.Thr591Ile)
NM_019842.4(KCNQ5):c.1948G>A (p.Glu650Lys)
NM_019842.4(KCNQ5):c.2074C>G (p.Leu692Val)
NM_019842.4(KCNQ5):c.2164G>A (p.Asp722Asn)
NM_019842.4(KCNQ5):c.2486C>G (p.Ser829Cys)
NM_019842.4(KCNQ5):c.2507T>A (p.Ile836Asn)	rs2150528291
NM_019842.4(KCNQ5):c.482T>C (p.Leu161Ser)	rs1342144805
NM_019842.4(KCNQ5):c.703C>T (p.Arg235Cys)	rs2150391522
NM_019842.4(KCNQ5):c.733A>G (p.Met245Val)

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