List of variants in gene ALDH7A1 reported as uncertain significance for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_001182.5(ALDH7A1):c.34del (p.Ala12fs)	rs750693623	0.00057
NM_001182.5(ALDH7A1):c.1150G>A (p.Ala384Thr)	rs140947675	0.00006
NM_001182.5(ALDH7A1):c.529G>C (p.Ala177Pro)	rs140102105	0.00006
NM_001182.5(ALDH7A1):c.364C>T (p.Arg122Trp)	rs370624118	0.00004
NM_001182.5(ALDH7A1):c.1489+4C>T	rs775065938	0.00003
NM_001182.5(ALDH7A1):c.998C>T (p.Ala333Val)	rs144625212	0.00003
NM_001182.5(ALDH7A1):c.1376T>C (p.Ile459Thr)	rs1057518529	0.00001
NM_001182.5(ALDH7A1):c.1301A>G (p.Tyr434Cys)	rs747597620
NM_001182.5(ALDH7A1):c.1A>G (p.Met1Val)
NM_001182.5(ALDH7A1):c.201G>T (p.Thr67=)	rs747643987
NM_001182.5(ALDH7A1):c.31_33delinsGAG (p.His11Glu)	rs796052269
NM_001182.5(ALDH7A1):c.50dup (p.Leu18fs)	rs1444879414
NM_001182.5(ALDH7A1):c.826A>C (p.Thr276Pro)	rs796052260
NM_001182.5(ALDH7A1):c.902A>G (p.Asn301Ser)	rs121912711

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