Variant (rsID / SNP)

rs13306061

rs13306061 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UTS2. Location: chromosome 1, position 7,913,445. The table records no clinical significance for this variant.

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Reference-table entries

UTS2Not classified

Variant type: missense_variant
Chromosome / position: 1:7913445
HGVS: NM_021995.2,c.47G>A,p.Arg16Gln
Allele change: Missense_R16Q

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.