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NM_015548.5(DST):c.3319-1492G>A AND Neuropathy, hereditary sensory and autonomic, type VI

Significance: Uncertain significance
ClinVar: RCV000260269

Variant: NM_015548.5(DST):c.3319-1492G>A

Type: Variant
Allele: NM_015548.5(DST):c.3319-1492G>A 303694
Gene:
Type: single nucleotide variant
Location: Chr6: 56615976 - assembly GRCh38
Chr6: 56480774 - assembly GRCh37
References: dbSNP: 145891100
Illumina Clinical Services Laboratory,Illumina: 599201

Condition

Disease: Neuropathy, hereditary sensory and autonomic, type VI