Variant (rsID / SNP)

rs11557064

rs11557064 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MPC1. Location: chromosome 6, position 166,780,349. Clinical significance in the table: Benign.

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Reference-table entries

MPC1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:166780349
Cytoband: 6q27
HGVS: NM_016098.4(MPC1):c.106C>A (p.Leu36Ile)
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.