Variant (rsID / SNP)

rs2070895

rs2070895 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LIPC. Location: chromosome 15, position 58,723,939. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LIPCBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:58723939
Cytoband: 15q21.3
HGVS: NM_000236.2(LIPC):c.-293G>A

Associated conditions / phenotypes

High density lipoprotein cholesterol level quantitative trait locus 12|Diabetes mellitus type 2, susceptibility to

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.