Variant (rsID / SNP)

rs33930274

rs33930274 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSHZ1. Location: chromosome 18, position 72,998,899. Clinical significance in the table: Benign.

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Reference-table entries

TSHZ1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 18:72998899
Cytoband: 18q22.3
HGVS: NM_001308210.2(TSHZ1):c.1537G>A (p.Ala513Thr)
Allele change: Missense_A468T

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.