Variant (rsID / SNP)

rs775882

rs775882 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NLRP7. Location: chromosome 19, position 55,451,232. Clinical significance in the table: Benign.

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Reference-table entries

NLRP7Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:55451232
Cytoband: 19q13.42
HGVS: NM_001127255.2(NLRP7):c.955G>A (p.Val319Ile)
Allele change: Missense_V319I

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.