Variant (rsID / SNP)

rs2294759

rs2294759 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VNN3P, VNN3. Location: chromosome 6, position 133,045,902. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

VNN3PNot classified

Variant type: non_coding_transcript_exon_variant
Chromosome / position: 6:133045902
HGVS: NR_173391.1,n.1164T>C
Allele change: Missense_F91S

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.