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NM_174934.3(SCN4B):c.568A>C (p.Ile190Leu) AND Long QT syndrome 10

Significance: Uncertain significance
ClinVar: RCV000646220

Variant: NM_174934.3(SCN4B):c.568A>C (p.Ile190Leu)

Type: Variant
Allele: NM_174934.3(SCN4B):c.568A>C (p.Ile190Leu) 526421
Gene:
Type: single nucleotide variant
Location: Chr11: 118011947 - assembly GRCh37
Chr11: 118141232 - assembly GRCh38
References: dbSNP: 757147726

Condition

Disease: Long QT syndrome 10