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NM_015548.5(DST):c.3220-3C>A AND Neuropathy, hereditary sensory and autonomic, type VI

Significance: Likely benign
ClinVar: RCV000265002

Variant: NM_015548.5(DST):c.3220-3C>A

Type: Variant
Allele: NM_015548.5(DST):c.3220-3C>A 308330
Gene:
Type: single nucleotide variant
Location: Chr6: 56624631 - assembly GRCh38
Chr6: 56489429 - assembly GRCh37
References: dbSNP: 115890942
Illumina Clinical Services Laboratory,Illumina: 730673

Condition

Disease: Neuropathy, hereditary sensory and autonomic, type VI