Variant (rsID / SNP)

rs3800592

rs3800592 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TMEM140. Location: chromosome 7, position 134,849,213. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TMEM140Not classified

Variant type: missense_variant
Chromosome / position: 7:134849213
HGVS: NM_018295.5,c.20G>A,p.Arg7Gln
Allele change: Silent

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.