Variant (rsID / SNP)

rs703473

rs703473 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NLRP7. Location: chromosome 19, position 55,458,816. The table records no clinical significance for this variant.

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Reference-table entries

NLRP7Not classified

Variant type: single nucleotide variant
Chromosome / position: 19:55458816
Cytoband: 19q13.42
HGVS: NM_001127255.1(NLRP7):c.-40+21C>T
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.