List of variants in gene TREM2 reported by Eurofins NTD LLC (GA)

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_018965.4(TREM2):c.632T>C (p.Leu211Pro)	rs2234256	0.04010
NM_018965.4(TREM2):c.*73G>A	rs2234258	0.01125
NM_018965.4(TREM2):c.185G>A (p.Arg62His)	rs143332484	0.00714
NM_018965.4(TREM2):c.469C>T (p.His157Tyr)	rs2234255	0.00187
NM_018965.4(TREM2):c.140G>A (p.Arg47His)	rs75932628	0.00153
NM_018965.4(TREM2):c.259G>A (p.Asp87Asn)	rs142232675	0.00152
NM_018965.4(TREM2):c.399G>T (p.Leu133=)	rs144250872	0.00095
NM_018965.4(TREM2):c.314C>T (p.Ala105Val)	rs145080901	0.00011
NM_018965.4(TREM2):c.407G>A (p.Arg136Gln)	rs149622783	0.00007
NM_018965.4(TREM2):c.204C>G (p.Asn68Lys)	rs753372932	0.00003
NM_018965.4(TREM2):c.677-6T>C	rs199910080	0.00002
NM_018965.4(TREM2):c.173G>A (p.Gly58Asp)	rs886042808
NM_018965.4(TREM2):c.287C>A (p.Thr96Lys)	rs2234253
NM_018965.4(TREM2):c.292C>T (p.Arg98Trp)	rs147564421
NM_018965.4(TREM2):c.431C>G (p.Pro144Arg)	rs1561877993

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