Variant (rsID / SNP)

rs883541

rs883541 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WIPI1, PRKAR1A. Location: chromosome 17, position 66,449,122. The table records no clinical significance for this variant.

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Reference-table entries

WIPI1Not classified

Variant type: missense_variant
Chromosome / position: 17:66449122
HGVS: NM_017983.7,c.92C>T,p.Thr31Ile
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.