Variant (rsID / SNP)

rs1128670

rs1128670 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MRPL18, TCP1. Location: chromosome 6, position 160,211,636. The table records no clinical significance for this variant.

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Reference-table entries

MRPL18Not classified

Variant type: missense_variant
Chromosome / position: 6:160211636
HGVS: NM_014161.5,c.17G>A,p.Arg6Gln
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.