Variant (rsID / SNP)

rs7258094

rs7258094 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPTBN4. Location: chromosome 19, position 41,012,190. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SPTBN4Not classified

Variant type: synonymous_variant
Chromosome / position: 19:41012190
HGVS: NM_020971.3,c.1713C>T,p.Asp571Asp
Allele change: Synonymous_D571D

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.