List of variants in gene MSX1 reported as likely benign for ectodermal dysplasia syndrome

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_002448.3(MSX1):c.821C>T (p.Ala274Val)	rs62636562	0.00031
NM_002448.3(MSX1):c.778C>A (p.Pro260Thr)	rs535538923	0.00021
NM_002448.3(MSX1):c.624G>T (p.Ser208=)	rs369820958	0.00007
NM_002448.3(MSX1):c.458C>A (p.Pro153Gln)	rs104893854	0.00003
NM_002448.3(MSX1):c.390G>T (p.Ala130=)
NM_002448.3(MSX1):c.426G>A (p.Arg142=)
NM_002448.3(MSX1):c.519T>C (p.Arg173=)
NM_002448.3(MSX1):c.526C>A (p.Arg176=)	rs1737946881
NM_002448.3(MSX1):c.624G>C (p.Ser208=)
NM_002448.3(MSX1):c.629G>A (p.Ser210Asn)
NM_002448.3(MSX1):c.912G>A (p.Ter304=)

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