List of variants in gene TREM2 reported as likely benign for autosomal recessive disease

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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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.399G>T (p.Leu133=)	rs144250872	0.00095
NM_018965.4(TREM2):c.*48A>T	rs200820365	0.00014
NM_018965.4(TREM2):c.514C>T (p.Pro172Ser)	rs781302866	0.00003
NM_018965.4(TREM2):c.287C>A (p.Thr96Lys)	rs2234253

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