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NM_174934.3(SCN4B):c.544C>G (p.Leu182Val) AND Long QT syndrome 10

Significance: Uncertain significance
ClinVar: RCV000467953

Variant: NM_174934.3(SCN4B):c.544C>G (p.Leu182Val)

Type: Variant
Allele: NM_174934.3(SCN4B):c.544C>G (p.Leu182Val) 398509
Gene:
Type: single nucleotide variant
Location: Chr11: 118011971 - assembly GRCh37
Chr11: 118141256 - assembly GRCh38
References: dbSNP: 771565684

Condition

Disease: Long QT syndrome 10