Variant (rsID / SNP)

rs914397

rs914397 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LINC02907. Location: chromosome 9, position 138,236,212. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LINC02907Not classified

Variant type: non_coding_transcript_exon_variant
Chromosome / position: 9:138236212
HGVS: NR_171012.1,n.568T>G
Allele change: Missense_W140G

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.