ClinVar Miner

List of variants in gene GRN reported as likely pathogenic for central nervous system disorder

Included ClinVar conditions (2490):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP gnomAD frequency
NM_002087.4(GRN):c.1179+1G>C
NM_002087.4(GRN):c.1179G>A (p.Glu393=) rs1567887777
NM_002087.4(GRN):c.1414-15_1591del
NM_002087.4(GRN):c.264+1G>A rs1567885728
NM_002087.4(GRN):c.265-2A>T
NM_002087.4(GRN):c.502_503insT (p.Gly168fs)
NM_002087.4(GRN):c.599-1G>A rs1555611154
NM_002087.4(GRN):c.835+1G>A rs606231221
NM_002087.4(GRN):c.933+1G>A rs63750707
NM_002087.4(GRN):c.934-11_936del
NM_002087.4(GRN):c.934-1G>A rs2143340416
NP_002078.1(GRN):p.Ser449_Thr455del

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