List of variants in gene SOBP reported as uncertain significance by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_018013.4(SOBP):c.1321C>T (p.Pro441Ser)	rs201319446	0.00176
NM_018013.4(SOBP):c.1810C>A (p.Gln604Lys)	rs368271940	0.00086
NM_018013.4(SOBP):c.573+12G>A	rs199899915	0.00066
NM_018013.4(SOBP):c.1729C>T (p.Pro577Ser)	rs200685194	0.00062
NM_018013.4(SOBP):c.2268G>A (p.Lys756=)	rs377096838	0.00040
NM_018013.4(SOBP):c.1747T>C (p.Ser583Pro)	rs760532040	0.00029
NM_018013.4(SOBP):c.265G>A (p.Glu89Lys)	rs200006380	0.00011
NM_018013.4(SOBP):c.2291C>T (p.Ala764Val)	rs372864608	0.00002
NM_018013.4(SOBP):c.1116C>T (p.Ile372=)	rs377312552	0.00001
NM_018013.4(SOBP):c.1118G>T (p.Gly373Val)	rs761861837	0.00001
NM_018013.4(SOBP):c.1896C>T (p.Gly632=)	rs797045998	0.00001
NM_018013.4(SOBP):c.219C>T (p.His73=)	rs759344534	0.00001
NM_018013.4(SOBP):c.2349C>T (p.Asp783=)	rs367899598	0.00001
NM_018013.4(SOBP):c.2412G>A (p.Pro804=)	rs797046001	0.00001
NM_018013.4(SOBP):c.2586A>T (p.Lys862Asn)	rs797046002	0.00001
NM_018013.4(SOBP):c.1905C>T (p.Gly635=)	rs587780465
NM_018013.4(SOBP):c.1937T>A (p.Leu646Gln)	rs1554190816
NM_018013.4(SOBP):c.1970C>G (p.Thr657Ser)	rs1554190839
NM_018013.4(SOBP):c.2105C>T (p.Ala702Val)	rs1554190937
NM_018013.4(SOBP):c.2232GCC[9] (p.Pro750_Pro751dup)	rs541688197
NM_018013.4(SOBP):c.2560C>G (p.Pro854Ala)	rs745943268
NM_018013.4(SOBP):c.413C>T (p.Pro138Leu)	rs1554288908
NM_018013.4(SOBP):c.414A>G (p.Pro138=)	rs1167539083

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