List of variants in gene SHOC2 reported as likely benign for Noonan syndrome-like disorder with loose anagen hair 1

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_007373.4(SHOC2):c.1423-7C>T	rs180671383	0.00563
NM_007373.4(SHOC2):c.*1062dup	rs530047047	0.00045
NM_007373.4(SHOC2):c.506_509del	rs371679867	0.00037
NM_007373.4(SHOC2):c.10A>C (p.Ser4Arg)	rs397517231	0.00004
NM_007373.4(SHOC2):c.38A>C (p.Glu13Ala)	rs730881018	0.00002
NM_007373.4(SHOC2):c.1215A>G (p.Val405=)	rs749123957	0.00001
NM_007373.4(SHOC2):c.303T>C (p.Asn101=)	rs750568201	0.00001
NM_007373.4(SHOC2):c.*1775del	rs527775221
NM_007373.4(SHOC2):c.703+15ATT[3]	rs370351651

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