ClinVar Miner

Variants in gene LINS1 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 6
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HGVS dbSNP gnomAD frequency
NM_001040616.3(LINS1):c.1285C>T (p.Leu429=) rs141962847 0.00463
NM_001040616.3(LINS1):c.718C>T (p.Arg240Trp) rs145145735 0.00398
NM_001040616.3(LINS1):c.1887C>T (p.Tyr629=) rs61999313 0.00313
NM_001040616.3(LINS1):c.1813A>G (p.Met605Val) rs141855950 0.00249
NM_001040616.3(LINS1):c.1194A>G (p.Gln398=) rs138347314 0.00244
NM_001040616.3(LINS1):c.2119G>A (p.Gly707Arg) rs74039425 0.00213

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