Variant (rsID / SNP)

rs12434757

rs12434757 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SYNE3. Location: chromosome 14, position 95,884,323. The table records no clinical significance for this variant.

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Reference-table entries

SYNE3Not classified

Variant type: missense_variant
Chromosome / position: 14:95884323
HGVS: NM_152592.6,c.2768C>T,p.Ala923Val
Allele change: Missense_A918V

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.