List of variants in gene TSHR reported as benign by PreventionGenetics, part of Exact Sciences

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000369.5(TSHR):c.2181G>C (p.Glu727Asp)	rs1991517	0.90865
NM_000369.5(TSHR):c.561T>C (p.Asn187=)	rs2075179	0.26593
NM_000369.5(TSHR):c.545+13A>G	rs2241119	0.26331
NM_000369.5(TSHR):c.2232C>G (p.Asn744Lys)	rs61743974	0.01750
NM_000369.5(TSHR):c.881+3A>G	rs186091357	0.00298
NM_000369.5(TSHR):c.1935G>A (p.Leu645=)	rs115815771	0.00247
NM_000369.5(TSHR):c.1377G>A (p.Ala459=)	rs113951800
NM_000369.5(TSHR):c.615-31TC[8]	rs3837640

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