ClinVar Miner

List of variants in gene NSD1 reported as likely benign for cardiovascular disorder

Included ClinVar conditions (1426):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_022455.5(NSD1):c.1797C>T (p.Ile599=) rs1554189107
NM_022455.5(NSD1):c.2148T>G (p.Thr716=) rs780294858
NM_022455.5(NSD1):c.7914C>T (p.Pro2638=) rs781650846

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