List of variants in gene HOXD13 reported as uncertain significance for non-syndromic synpolydactyly

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000523.4(HOXD13):c.170C>T (p.Ala57Val)	rs755283984	0.00006
NM_000523.4(HOXD13):c.202G>C (p.Ala68Pro)	rs760168666
NM_000523.4(HOXD13):c.296C>G (p.Pro99Arg)	rs143487752
NM_000523.4(HOXD13):c.623A>T (p.Asp208Val)	rs2105379098
NM_000523.4(HOXD13):c.709G>C (p.Gly237Arg)	rs1689365853

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