List of variants in gene LAMA3 reported by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 22

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HGVS	dbSNP	gnomAD frequency
NM_198129.4(LAMA3):c.8445C>A (p.Asn2815Lys)	rs1154232	0.17201
NM_198129.4(LAMA3):c.5322C>T (p.Phe1774=)	rs958631	0.08419
NM_198129.4(LAMA3):c.8851C>T (p.Arg2951Cys)	rs61752346	0.00147
NM_198129.4(LAMA3):c.5780C>T (p.Thr1927Ile)	rs146039146	0.00019
NM_198129.4(LAMA3):c.8162T>C (p.Ile2721Thr)	rs144798744	0.00005
NM_198129.4(LAMA3):c.8192C>T (p.Thr2731Met)	rs776754771	0.00002
NM_198129.4(LAMA3):c.5872G>T (p.Gly1958Ter)	rs2080986242	0.00001
NM_198129.4(LAMA3):c.6407C>T (p.Thr2136Ile)	rs370749309	0.00001
NM_198129.4(LAMA3):c.7204C>T (p.Arg2402Ter)	rs777713989	0.00001
NM_198129.4(LAMA3):c.7627T>C (p.Tyr2543His)	rs778189535	0.00001
NM_198129.4(LAMA3):c.8203C>T (p.Arg2735Ter)	rs774133746	0.00001
NM_198129.4(LAMA3):c.9511+1G>A	rs1296034886	0.00001
NM_198129.4(LAMA3):c.5546del (p.Gly1849fs)	rs760487161
NM_198129.4(LAMA3):c.5632C>T (p.Arg1878Cys)	rs867507379
NM_198129.4(LAMA3):c.6232_6233del (p.Gln2077_Ser2078insTer)	rs1158945258
NM_198129.4(LAMA3):c.6281C>A (p.Thr2094Asn)	rs2145140189
NM_198129.4(LAMA3):c.6976G>C (p.Glu2326Gln)	rs148831718
NM_198129.4(LAMA3):c.7828C>T (p.Arg2610Ter)	rs768415785
NM_198129.4(LAMA3):c.8178-1G>C	rs1047102588
NM_198129.4(LAMA3):c.8295+1_8295+11del
NM_198129.4(LAMA3):c.8708+4G>A	rs200417639
NM_198129.4(LAMA3):c.8862+1G>A

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