Variant (rsID / SNP)

rs2282397

rs2282397 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPATA46. Location: chromosome 1, position 162,344,102. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SPATA46Not classified

Variant type: synonymous_variant
Chromosome / position: 1:162344102
HGVS: NM_182581.4,c.522G>A,p.Arg174Arg
Allele change: Synonymous_R174R

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.