Variant (rsID / SNP)

rs17032441

rs17032441 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SYT6. Location: chromosome 1, position 114,680,540. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SYT6Not classified

Variant type: synonymous_variant
Chromosome / position: 1:114680540
HGVS: NM_001366224.1,c.648G>A,p.Ser216Ser
Allele change: Synonymous_S131S

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.