List of variants in gene combination MAP2K1, SNAPC5 reported as uncertain significance for bone disorder

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_002755.4(MAP2K1):c.1062A>C (p.Gln354His)	rs750035241	0.00002
NM_002755.4(MAP2K1):c.1177G>A (p.Val393Ile)	rs200442489	0.00002
NM_002755.4(MAP2K1):c.1135A>G (p.Ile379Val)	rs373794940	0.00001
NM_002755.4(MAP2K1):c.*17A>T
NM_002755.4(MAP2K1):c.1068+5G>A
NM_002755.4(MAP2K1):c.1166A>G (p.His389Arg)

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