List of variants in gene NTRK1 reported as likely 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: 27

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HGVS	dbSNP	gnomAD frequency
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.53G>A (p.Gly18Glu)	rs1007211	0.00957
NM_002529.4(NTRK1):c.2339G>A (p.Arg780Gln)	rs35669708	0.00406
NM_002529.4(NTRK1):c.1236C>T (p.Asp412=)	rs147438950	0.00289
NM_002529.4(NTRK1):c.612G>A (p.Ser204=)	rs114320051	0.00251
NM_002529.4(NTRK1):c.254G>A (p.Arg85His)	rs79678945	0.00220
NM_002529.4(NTRK1):c.*7G>T	rs145060242	0.00210
NM_002529.4(NTRK1):c.865C>A (p.Gln289Lys)	rs137979116	0.00118
NM_002529.4(NTRK1):c.1252-15C>G	rs186649954	0.00049
NM_002529.4(NTRK1):c.1068C>T (p.Asn356=)	rs145823996	0.00029
NM_002529.4(NTRK1):c.574+10G>A	rs201336491	0.00026
NM_002529.4(NTRK1):c.927G>A (p.Pro309=)	rs144015813	0.00018
NM_002529.4(NTRK1):c.1257G>A (p.Ser419=)	rs750968694	0.00012
NM_002529.4(NTRK1):c.279G>A (p.Leu93=)	rs147983523	0.00011
NM_002529.4(NTRK1):c.575-16C>T	rs143312136	0.00009
NM_002529.4(NTRK1):c.1522C>A (p.Arg508=)	rs200575096	0.00006
NM_002529.4(NTRK1):c.1354+8G>A	rs763576316	0.00003
NM_002529.4(NTRK1):c.2169C>T (p.Tyr723=)	rs140852621	0.00002
NM_002529.4(NTRK1):c.531T>C (p.Cys177=)	rs1057523619	0.00002
NM_002529.4(NTRK1):c.2047-6T>C	rs762866535	0.00001
NM_002529.4(NTRK1):c.2067G>A (p.Leu689=)	rs1057521447	0.00001
NM_002529.4(NTRK1):c.718-15T>C	rs778745696	0.00001
NM_002529.4(NTRK1):c.1077C>T (p.Tyr359=)	rs1057521034
NM_002529.4(NTRK1):c.291C>T (p.Thr97=)	rs1057522997
NM_002529.4(NTRK1):c.321G>T (p.Ala107=)	rs774351278
NM_002529.4(NTRK1):c.428+12C>T	rs41267425

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