ClinVar Miner

List of variants reported as uncertain significance for Seckel syndrome 1 by Mendelics

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Total variants: 3

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HGVS	dbSNP
NM_001184.4(ATR):c.2305C>A (p.Leu769Ile)	rs1489808838
NM_001184.4(ATR):c.6259A>G (p.Met2087Val)	rs757353909
NM_018451.5(CENPJ):c.2462C>T (p.Thr821Met)	rs144938364

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