Variant (rsID / SNP)

rs61750008

rs61750008 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAS2R60, EPHA1-AS1. Location: chromosome 7, position 143,140,675. The table records no clinical significance for this variant.

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Reference-table entries

TAS2R60Not classified

Variant type: missense_variant
Chromosome / position: 7:143140675
HGVS: NM_177437.1,c.130G>A,p.Val44Met
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.