Variant (rsID / SNP)

rs17417442

rs17417442 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM72, TMEM72-AS1. Location: chromosome 10, position 45,430,462. The table records no clinical significance for this variant.

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Reference-table entries

TMEM72Not classified

Variant type: synonymous_variant
Chromosome / position: 10:45430462
HGVS: NM_001123376.3,c.708C>T,p.Ala236Ala
Allele change: Silent

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.