Variant (rsID / SNP)

rs4982766

rs4982766 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZFHX2, THTPA. Location: chromosome 14, position 23,994,517. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ZFHX2Not classified

Variant type: missense_variant
Chromosome / position: 14:23994517
HGVS: NM_033400.3,c.4634T>C,p.Val1545Ala
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.