Variant (rsID / SNP)

rs2073721

rs2073721 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TCF19. Location: chromosome 6, position 31,129,616. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TCF19Not classified

Variant type: missense_variant
Chromosome / position: 6:31129616
HGVS: NM_001077511.2,c.631A>G,p.Met211Val
Allele change: Missense_M211V

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.