List of variants in gene SORD reported by Mayo Clinic Laboratories, Mayo Clinic

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_003104.6(SORD):c.274G>C (p.Val92Leu)	rs754260257	0.00005
NM_003104.6(SORD):c.286C>T (p.Pro96Ser)
NM_003104.6(SORD):c.481G>A (p.Gly161Arg)
NM_003104.6(SORD):c.67_69del	rs1566959066
NM_003104.6(SORD):c.698C>T (p.Ala233Val)
NM_003104.6(SORD):c.757del (p.Ala253fs)	rs55901542
NM_003104.6(SORD):c.868C>T (p.Arg290Trp)

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