Variant (rsID / SNP)

rs2668424

rs2668424 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PWWP3A. Location: chromosome 19, position 1,371,354. The table records no clinical significance for this variant.

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Reference-table entries

PWWP3ANot classified

Variant type: intron_variant
Chromosome / position: 19:1371354
HGVS: NM_001369790.1,c.1986+277T>C
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.