List of variants in gene LAMA3 studied for not specified

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_198129.4(LAMA3):c.8500= (p.Gly2834=)	rs1154233	0.99993
NM_198129.4(LAMA3):c.2901T>C (p.Ala967=)	rs9962023	0.64176
NM_198129.4(LAMA3):c.9211-21C>T	rs2288592	0.51885
NM_198129.4(LAMA3):c.9352-7G>A	rs2241643	0.51794
NM_198129.4(LAMA3):c.4260G>C (p.Gly1420=)	rs867449	0.48275
NM_198129.4(LAMA3):c.4530C>T (p.Pro1510=)	rs12965685	0.47260
NM_198129.4(LAMA3):c.6147C>G (p.Ala2049=)	rs1154226	0.21073
NM_198129.4(LAMA3):c.8445C>A (p.Asn2815Lys)	rs1154232	0.17201
NM_198129.4(LAMA3):c.8731C>T (p.Leu2911=)	rs1131521	0.15145
NM_198129.4(LAMA3):c.5322C>T (p.Phe1774=)	rs958631	0.08419
NM_198129.4(LAMA3):c.9353G>A (p.Ser3118Asn)	rs61749943	0.00618
NM_198129.4(LAMA3):c.7797C>T (p.Asp2599=)	rs61751706	0.00523
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.6407C>T (p.Thr2136Ile)	rs370749309	0.00001
NM_198129.4(LAMA3):c.7627T>C (p.Tyr2543His)	rs778189535	0.00001
NM_198129.4(LAMA3):c.5632C>T (p.Arg1878Cys)	rs867507379
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.8576+7G>C	rs1258107
NM_198129.4(LAMA3):c.8708+4G>A	rs200417639

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