ClinVar Miner

List of variants reported as likely pathogenic for Noonan syndrome by Genomic Research Center,Shahid Beheshti University of Medical Sciences

Included ClinVar conditions (28):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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HGVS dbSNP
NM_002834.4(PTPN11):c.959A>G (p.Asn320Ser) rs1398859175
NM_004333.6(BRAF):c.1387A>G (p.Ile463Val) rs1562957000

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