Variant (rsID / SNP)

rs7716253

rs7716253 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARHGEF28. Location: chromosome 5, position 73,090,261. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ARHGEF28Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:73090261
Cytoband: 5q13.2
HGVS: NM_001177693.2(ARHGEF28):c.945T>C (p.Ala315=)
Allele change: Synonymous_A315A

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.