GENETIC ENCYCLOPEDIA
ABOUT US    

   

NM_015548.5(DST):c.3319-438G>C AND Neuropathy, hereditary sensory and autonomic, type VI

Significance: Uncertain significance
ClinVar: RCV000259792

Variant: NM_015548.5(DST):c.3319-438G>C

Type: Variant
Allele: NM_015548.5(DST):c.3319-438G>C 303683
Gene:
Type: single nucleotide variant
Location: Chr6: 56614922 - assembly GRCh38
Chr6: 56479720 - assembly GRCh37
References: dbSNP: 145471325
Illumina Clinical Services Laboratory,Illumina: 766769

Condition

Disease: Neuropathy, hereditary sensory and autonomic, type VI