Variant (rsID / SNP)

rs7975161

rs7975161 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TXNRD1. Location: chromosome 12, position 104,645,405. The table records no clinical significance for this variant.

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Reference-table entries

TXNRD1Not classified

Variant type: synonymous_variant
Chromosome / position: 12:104645405
HGVS: NM_001093771.3,c.192T>C,p.Asp64Asp
Allele change: Synonymous_D64D

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.