List of variants in gene LAMA3 reported as benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_198129.4(LAMA3):c.8500= (p.Gly2834=)	rs1154233	0.99993
NM_198129.4(LAMA3):c.9352-7G>A	rs2241643	0.51794
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.3066C>G (p.Leu1022=)	rs35756007	0.03848
NM_198129.4(LAMA3):c.8104A>G (p.Thr2702Ala)	rs9952370	0.01207
NM_198129.4(LAMA3):c.1806G>A (p.Lys602=)	rs34713637	0.00662
NM_198129.4(LAMA3):c.6805C>G (p.Leu2269Val)	rs138591939	0.00303
NM_198129.4(LAMA3):c.8629C>T (p.His2877Tyr)	rs35153125	0.00264
NM_198129.4(LAMA3):c.4060G>A (p.Glu1354Lys)	rs34799994	0.00224
NM_198129.4(LAMA3):c.2996G>A (p.Arg999Gln)	rs199976293	0.00034
NM_198129.4(LAMA3):c.9165G>A (p.Leu3055=)	rs370470226	0.00018
NM_198129.4(LAMA3):c.1831A>C (p.Ser611Arg)
NM_198129.4(LAMA3):c.4545C>T (p.Ser1515=)
NM_198129.4(LAMA3):c.4584+14G>A
NM_198129.4(LAMA3):c.8576+7G>C	rs1258107

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