Variant (rsID / SNP)

rs3741132

rs3741132 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to P4HA3. Location: chromosome 11, position 73,978,243. The table records no clinical significance for this variant.

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Reference-table entries

P4HA3Not classified

Variant type: stop_gained
Chromosome / position: 11:73978243
HGVS: NM_001288748.2,c.1678C>T,p.Gln560*
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.