List of variants in gene combination NTRK1, SH2D2A

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_003975.4(SH2D2A):c.124-343A>G	rs2150906	0.85065
NM_003975.4(SH2D2A):c.123+19C>T	rs1800600	0.64949
NM_003975.4(SH2D2A):c.123+27T>C	rs7546838	0.58984
NM_003975.4(SH2D2A):c.123+35del	rs11325907	0.55268
NM_003975.4(SH2D2A):c.123+65A>G	rs139790457	0.00640
NM_003975.4(SH2D2A):c.111G>C (p.Leu37=)	rs145574758	0.00404
NM_003975.4(SH2D2A):c.84C>T (p.Asp28=)	rs146503193	0.00012
NM_003975.4(SH2D2A):c.123+181C>T	rs1800601
NM_003975.4(SH2D2A):c.123+185T>C
NM_003975.4(SH2D2A):c.123+253del	rs146775862

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