List of variants in gene combination LOC126807125, SLC39A8 reported as uncertain significance for central nervous system malformation

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001135146.2(SLC39A8):c.1166A>G (p.Asn389Ser)	rs146759817	0.00032
NM_001135146.2(SLC39A8):c.923C>T (p.Thr308Met)	rs376000562	0.00004
NM_001135146.2(SLC39A8):c.965T>C (p.Ile322Thr)	rs755786784	0.00001
NM_001135146.2(SLC39A8):c.1020C>G (p.Ile340Met)	rs1732174032
NM_001135146.2(SLC39A8):c.1097dup (p.Leu366fs)	rs1553911693
NM_001135146.2(SLC39A8):c.1120T>A (p.Cys374Ser)
NM_001135146.2(SLC39A8):c.915G>C (p.Trp305Cys)	rs1578557666

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