Variant (rsID / SNP)

rs13392363

rs13392363 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LPIN1. Location: chromosome 2, position 11,925,335. Clinical significance in the table: Benign.

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Reference-table entries

LPIN1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:11925335
Cytoband: 2p25.1
HGVS: NM_001349206.2(LPIN1):c.1549+133A>G
Allele change: Silent

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.