ClinVar Miner

List of variants in gene combination LOC101927870, RELN reported as likely benign for Norman-Roberts syndrome

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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NM_005045.4(RELN):c.10108A>G (p.Thr3370Ala) rs570807790
NM_005045.4(RELN):c.8951-11_8951-8dup rs1554364085
NM_005045.4(RELN):c.9105G>A (p.Gly3035=) rs1279644782
NM_005045.4(RELN):c.9172T>C (p.Leu3058=) rs2286261
NM_005045.4(RELN):c.9414C>T (p.Ser3138=) rs375427974
NM_005045.4(RELN):c.9984-9G>A rs758320422

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