Variant (rsID / SNP)

rs3806164

rs3806164 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARHGEF16. Location: chromosome 1, position 3,380,057. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ARHGEF16Not classified

Variant type: missense_variant
Chromosome / position: 1:3380057
HGVS: NM_014448.4,c.409G>A,p.Val137Met
Allele change: Missense_V137M

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.