Variant (rsID / SNP)

rs1255953

rs1255953 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SYNE2. Location: chromosome 14, position 64,551,688. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SYNE2Not classified

Variant type: intron_variant
Chromosome / position: 14:64551688
HGVS: NM_182914.3,c.11485-2701C>T
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.