Variant (rsID / SNP)

rs145970530

rs145970530 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAS2R38. Location: chromosome 7, position 141,673,074. The table records no clinical significance for this variant.

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Reference-table entries

TAS2R38Not classified

Variant type: missense_variant
Chromosome / position: 7:141673074
HGVS: NM_176817.5,c.416A>G,p.Lys139Arg
Allele change: Missense_K139R

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.