List of variants in gene LGR5 studied for not provided

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_003667.4(LGR5):c.2341C>G (p.Pro781Ala)	rs113809442	0.00718
NM_003667.4(LGR5):c.1282G>A (p.Asp428Asn)	rs146110108	0.00535
NM_003667.4(LGR5):c.1270C>G (p.Leu424Val)	rs138215571	0.00481
NM_003667.4(LGR5):c.653A>G (p.His218Arg)	rs117535164	0.00287
NM_003667.4(LGR5):c.1148A>G (p.His383Arg)	rs12303775	0.00243
NM_003667.4(LGR5):c.1304C>T (p.Ser435Leu)	rs73339868	0.00188
NM_003667.4(LGR5):c.2031A>G (p.Pro677=)	rs138932490	0.00172
NM_003667.4(LGR5):c.384C>T (p.His128=)	rs142698551	0.00048
GRCh37/hg19 12q21.1(chr12:71722986-71973110)x4
GRCh37/hg19 12q21.1(chr12:71722986-71978728)x3
NM_003667.4(LGR5):c.1290G>T (p.Ser430=)	rs80013431

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