Variant (rsID / SNP)

rs10923472

rs10923472 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPAG17. Location: chromosome 1, position 118,565,953. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SPAG17Not classified

Variant type: missense_variant
Chromosome / position: 1:118565953
HGVS: NM_206996.4,c.4043C>T,p.Pro1348Leu
Allele change: Missense_P1348L

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.