ClinVar Miner

List of variants in gene ARHGEF10 reported as likely benign for Slowed nerve conduction velocity, autosomal dominant

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Total variants: 4
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NM_014629.4(ARHGEF10):c.2259+8T>C rs1015159398
NM_014629.4(ARHGEF10):c.2812G>A (p.Val938Ile) rs61752020
NM_014629.4(ARHGEF10):c.2909C>T (p.Thr970Met) rs35925274
NM_014629.4(ARHGEF10):c.38-10T>C rs138713415

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