Variant (rsID / SNP)

rs79711969

rs79711969 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NLRP7, NCR1. Location: chromosome 19, position 55,439,702. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

NLRP7Not classified

Variant type: single nucleotide variant
Chromosome / position: 19:55439702
Cytoband: 19q13.42
HGVS: NM_001127255.1(NLRP7):c.2811-559A>G
Allele change: Silent

Associated conditions / phenotypes

Hydatidiform mole, recurrent, 1

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.