List of variants in gene SH3TC2 reported as uncertain significance by Baylor Genetics

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_024577.4(SH3TC2):c.3380G>A (p.Arg1127Gln)	rs139192433	0.00108
NM_024577.4(SH3TC2):c.2990G>A (p.Arg997Gln)	rs140307699	0.00047
NM_024577.4(SH3TC2):c.794C>T (p.Ser265Phe)	rs149873249	0.00032
NM_024577.4(SH3TC2):c.3213C>T (p.Ile1071=)	rs1753764451
NM_024577.4(SH3TC2):c.3804C>T (p.Ser1268=)	rs1434453673
NM_024577.4(SH3TC2):c.910G>A (p.Gly304Arg)	rs1754317705

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