Variant (rsID / SNP)

rs416574

rs416574 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TRIM7. Location: chromosome 5, position 180,626,927. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TRIM7Not classified

Variant type: missense_variant
Chromosome / position: 5:180626927
HGVS: NM_203293.3,c.773T>C,p.Val258Ala
Allele change: Missense_V50A

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.