List of variants in gene SHOC2 reported as likely pathogenic for loose anagen 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_007373.4(SHOC2):c.1439A>C (p.Asn480Thr)	rs995403413	0.00001
NM_007373.4(SHOC2):c.4A>G (p.Ser2Gly)	rs267607048	0.00001
NM_007373.4(SHOC2):c.157G>A (p.Gly53Arg)	rs2134121169
NM_007373.4(SHOC2):c.517A>G (p.Met173Val)	rs1057518206
NM_007373.4(SHOC2):c.519G>A (p.Met173Ile)	rs730881020
NM_007373.4(SHOC2):c.806A>G (p.Gln269Arg)	rs864309599

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