List of variants in gene HSPG2 reported by Baylor Genetics

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_005529.7(HSPG2):c.2357A>G (p.Asn786Ser)	rs143736974	0.00628
NM_005529.7(HSPG2):c.4916C>T (p.Thr1639Met)	rs142433309	0.00177
NM_005529.7(HSPG2):c.2335C>T (p.His779Tyr)	rs149094407	0.00086
NM_005529.7(HSPG2):c.7423G>C (p.Gly2475Arg)	rs142601663	0.00032
NM_005529.7(HSPG2):c.8025+20C>T	rs146363738	0.00023
NM_005529.7(HSPG2):c.4928C>A (p.Pro1643His)	rs775389963	0.00006
NM_005529.7(HSPG2):c.5350C>T (p.Arg1784Cys)	rs150937055	0.00004
NM_005529.7(HSPG2):c.7775C>T (p.Pro2592Leu)	rs140341550	0.00004
NM_005529.7(HSPG2):c.916G>A (p.Gly306Arg)	rs149899316	0.00004
NM_005529.7(HSPG2):c.1834G>A (p.Gly612Ser)	rs768946900	0.00003
NM_005529.7(HSPG2):c.3875A>G (p.Gln1292Arg)	rs764233594	0.00003
NM_005529.7(HSPG2):c.1666A>T (p.Thr556Ser)	rs769587805	0.00001
NM_005529.7(HSPG2):c.4040A>C (p.His1347Pro)	rs1234473043	0.00001
NM_005529.7(HSPG2):c.9958T>C (p.Cys3320Arg)	rs2098038156

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