Variant (rsID / SNP)

rs145178162

rs145178162 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PNPLA6. Location: chromosome 19, position 7,626,428. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

PNPLA6Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 19:7626428
Cytoband: 19p13.2
HGVS: NM_001166114.2(PNPLA6):c.4078G>A (p.Gly1360Ser)
Allele change: Missense_G1322S

Associated conditions / phenotypes

Hereditary spastic paraplegia 39|Hereditary spastic paraplegia

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.