Variant (rsID / SNP)

rs2254067

rs2254067 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TASOR2. Location: chromosome 10, position 5,781,628. The table records no clinical significance for this variant.

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Reference-table entries

TASOR2Not classified

Variant type: missense_variant
Chromosome / position: 10:5781628
HGVS: NM_001387328.1,c.2140T>G,p.Cys714Gly
Allele change: Missense_C499G

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.