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Variant (rsID / SNP)

rs41290259

TASOR2

rs41290259 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TASOR2. Location: chromosome 10, position 5,803,368. The table records no clinical significance for this variant.

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Reference-table entries

TASOR2Not classified
Variant type
missense_variant
Chromosome / position
10:5803368
HGVS
NM_001387328.1,c.7753A>G,p.Ile2585Val
Allele change
Missense_I2370V

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.