ClinVar Miner

List of variants in gene NIN reported as benign for Seckel syndrome

Included ClinVar conditions (16):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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NM_016350.4(NIN):c.2399+2201A>C rs12882191
NM_016350.4(NIN):c.2400-2204G>A rs2073347
NM_020921.3(NIN):c.5800C>G (p.Gln1934Glu) rs2295847

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