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NM_015548.5(DST):c.3318+4452C>A AND Neuropathy, hereditary sensory and autonomic, type VI

Significance: Uncertain significance
ClinVar: RCV000292950

Variant: NM_015548.5(DST):c.3318+4452C>A

Type: Variant
Allele: NM_015548.5(DST):c.3318+4452C>A 308308
Gene:
Type: single nucleotide variant
Location: Chr6: 56620078 - assembly GRCh38
Chr6: 56484876 - assembly GRCh37
References: dbSNP: 142302277
Illumina Clinical Services Laboratory,Illumina: 647636

Condition

Disease: Neuropathy, hereditary sensory and autonomic, type VI