List of variants in gene SHOC2 reported by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_007373.4(SHOC2):c.457C>T (p.Leu153=)	rs34081996	0.01281
NM_007373.4(SHOC2):c.1423-7C>T	rs180671383	0.00563
NM_007373.4(SHOC2):c.704-16G>T	rs185614302	0.00033
NM_007373.4(SHOC2):c.74A>G (p.Glu25Gly)	rs730881019	0.00008
NM_007373.4(SHOC2):c.10A>C (p.Ser4Arg)	rs397517231	0.00004
NM_007373.4(SHOC2):c.170C>T (p.Ser57Phe)	rs536611911	0.00003
NM_007373.4(SHOC2):c.38A>C (p.Glu13Ala)	rs730881018	0.00002
NM_007373.4(SHOC2):c.303T>C (p.Asn101=)	rs750568201	0.00001
NM_007373.4(SHOC2):c.4A>G (p.Ser2Gly)	rs267607048	0.00001
NM_007373.4(SHOC2):c.1541-7del	rs371544139

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