Variant (rsID / SNP)

rs117077213

rs117077213 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRPPRC. Location: chromosome 2, position 44,152,190. Clinical significance in the table: Benign.

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Reference-table entries

LRPPRCBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 2:44152190
Cytoband: 2p21
HGVS: NM_133259.4(LRPPRC):c.2896+16A>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.