ClinVar Miner

List of variants in gene LAMA3 reported as benign for Laryngo-onycho-cutaneous syndrome

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Total variants: 33
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HGVS dbSNP gnomAD frequency
NM_198129.4(LAMA3):c.8500= (p.Gly2834=) rs1154233 0.99993
NM_198129.4(LAMA3):c.2304+67G>T rs6507956 0.79861
NM_198129.4(LAMA3):c.1942-74G>C rs2155841 0.79748
NM_198129.4(LAMA3):c.948-84C>T rs6507894 0.72706
NM_198129.4(LAMA3):c.7778+97T>C rs1541836 0.67847
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.*91C>T rs1051150 0.51640
NM_198129.4(LAMA3):c.*89C>A rs1051149 0.51636
NM_198129.4(LAMA3):c.4260G>C (p.Gly1420=) rs867449 0.48275
NM_198129.4(LAMA3):c.4137-87A>G rs867448 0.47865
NM_198129.4(LAMA3):c.2304+44A>C rs7244406 0.47571
NM_198129.4(LAMA3):c.4530C>T (p.Pro1510=) rs12965685 0.47260
NM_198129.4(LAMA3):c.6201+53A>G rs1154227 0.35521
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.1183-110C>T rs6507907 0.16922
NM_198129.4(LAMA3):c.565+64G>T rs9955745 0.15790
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.6555C>T (p.Ala2185=) rs35872318 0.02513
NM_198129.4(LAMA3):c.*239G>A rs45543834 0.01494
NM_198129.4(LAMA3):c.8104A>G (p.Thr2702Ala) rs9952370 0.01207
NM_198129.4(LAMA3):c.9643-14C>T rs72875942 0.00748
NM_198129.4(LAMA3):c.9353G>A (p.Ser3118Asn) rs61749943 0.00618
NM_198129.4(LAMA3):c.*395A>T rs138907590 0.00519
NM_198129.4(LAMA3):c.7818G>A (p.Thr2606=) rs139567388 0.00426
NM_198129.4(LAMA3):c.9027-11G>A rs117781425 0.00152
NM_198129.4(LAMA3):c.8898C>T (p.Ser2966=) rs141164795 0.00121
NM_198129.4(LAMA3):c.1064-15A>G rs7232856
NM_198129.4(LAMA3):c.5462-44G>A rs1268716
NM_198129.4(LAMA3):c.8576+7G>C rs1258107

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