ClinVar Miner

List of variants in gene LAMB1 reported as likely benign for not specified

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Gene type:
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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_002291.3(LAMB1):c.3012G>A (p.Thr1004=) rs113725211 0.00487
NM_002291.3(LAMB1):c.1370-18C>T rs79590733 0.00436
NM_002291.3(LAMB1):c.4221C>T (p.Ser1407=) rs35082294 0.00416
NM_002291.3(LAMB1):c.2542G>C (p.Ala848Pro) rs145746791 0.00371
NM_002291.3(LAMB1):c.1590A>C (p.Ser530=) rs139481973 0.00175
NM_002291.3(LAMB1):c.1483-14G>A rs115559402 0.00073
NM_002291.3(LAMB1):c.2691-9C>T rs751631641 0.00044
NM_002291.3(LAMB1):c.1482+19C>T rs376329632 0.00023
NM_002291.3(LAMB1):c.3642G>T (p.Gly1214=) rs569355700 0.00021
NM_002291.3(LAMB1):c.1074C>T (p.Ser358=) rs758179734 0.00011
NM_002291.3(LAMB1):c.349+19G>A rs756720953 0.00011
NM_002291.3(LAMB1):c.816C>T (p.Phe272=) rs562088411 0.00007
NM_002291.3(LAMB1):c.3498G>A (p.Thr1166=) rs778237047 0.00006
NM_002291.3(LAMB1):c.3444G>A (p.Thr1148=) rs753168303 0.00004
NM_002291.3(LAMB1):c.3639C>T (p.Ile1213=) rs141885441 0.00004
NM_002291.3(LAMB1):c.5325A>T (p.Ile1775=) rs369528849 0.00004
NM_002291.3(LAMB1):c.3762-4A>G rs374438596 0.00002
NM_002291.3(LAMB1):c.3834C>T (p.Ser1278=) rs1389549765 0.00002
NM_002291.3(LAMB1):c.5268T>C (p.Asp1756=) rs149602697 0.00002
NM_002291.3(LAMB1):c.1944C>T (p.Pro648=) rs751175194 0.00001
NM_002291.3(LAMB1):c.1977A>G (p.Pro659=) rs1057523829
NM_002291.3(LAMB1):c.1985+11C>G rs192349543
NM_002291.3(LAMB1):c.2684G>A (p.Cys895Tyr) rs1554406824
NM_002291.3(LAMB1):c.3300G>A (p.Thr1100=) rs139955747
NM_002291.3(LAMB1):c.3946+16T>C rs777888220
NM_002291.3(LAMB1):c.4074C>T (p.Asp1358=) rs146681738
NM_002291.3(LAMB1):c.981A>T (p.Arg327=) rs1554410490

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