Variant (rsID / SNP)

rs2296700

rs2296700 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCNX4. Location: chromosome 14, position 60,574,448. The table records no clinical significance for this variant.

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Reference-table entries

PCNX4Not classified

Variant type: missense_variant
Chromosome / position: 14:60574448
HGVS: NM_001330177.2,c.92A>G,p.Lys31Arg
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.