List of variants in gene NTRK1 reported as benign for not specified

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_002529.4(NTRK1):c.1887C>T (p.Ala629=)	rs6337	0.53946
NM_002529.4(NTRK1):c.1674G>A (p.Gln558=)	rs6334	0.19892
NM_002529.4(NTRK1):c.2047-16T>C	rs12076232	0.10434
NM_002529.4(NTRK1):c.1838G>T (p.Gly613Val)	rs6339	0.03698
NM_002529.4(NTRK1):c.1810C>T (p.His604Tyr)	rs6336	0.03696
NM_002529.4(NTRK1):c.1860C>T (p.Gly620=)	rs6338	0.03397
NM_002529.4(NTRK1):c.2052A>G (p.Gly684=)	rs34271945	0.03311
NM_002529.4(NTRK1):c.710C>T (p.Thr237Met)	rs55909005	0.01791
NM_002529.4(NTRK1):c.1331G>A (p.Arg444Gln)	rs56320207	0.01010
NM_002529.4(NTRK1):c.53G>A (p.Gly18Glu)	rs1007211	0.00957
NM_002529.4(NTRK1):c.288-8C>T	rs80026148	0.00947
NM_002529.4(NTRK1):c.2202G>A (p.Thr734=)	rs55668752	0.00562
NM_002529.4(NTRK1):c.2339G>A (p.Arg780Gln)	rs35669708	0.00406
NM_002529.4(NTRK1):c.428+12C>A	rs41267425	0.00357
NM_002529.4(NTRK1):c.254G>A (p.Arg85His)	rs79678945	0.00220
NM_002529.4(NTRK1):c.212+10C>T	rs183517027	0.00108
NM_002529.4(NTRK1):c.117C>T (p.Ala39=)	rs746293720	0.00003

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