ClinVar Miner

List of variants in gene RELN reported as benign for Norman-Roberts syndrome

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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NM_005045.4(RELN):c.1290-3del rs146986040
NM_005045.4(RELN):c.1596G>A (p.Gln532=) rs41276154
NM_005045.4(RELN):c.1799C>T (p.Ser600Phe) rs78008536
NM_005045.4(RELN):c.1888A>C (p.Ser630Arg) rs115734214
NM_005045.4(RELN):c.2932A>G (p.Thr978Ala) rs3025962
NM_005045.4(RELN):c.3651C>G (p.Ile1217Met) rs56342240
NM_005045.4(RELN):c.4937-14_4937-13dup rs35268159
NM_005045.4(RELN):c.4937-4del rs35268159
NM_005045.4(RELN):c.578-3T>C rs607755
NM_005045.4(RELN):c.7110T>C (p.Val2370=) rs362746
NM_005045.4(RELN):c.7887T>C (p.Pro2629=) rs56345626
NM_005045.4(RELN):c.8046T>C (p.His2682=) rs2229864

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