Variant (rsID / SNP)

rs5924977

rs5924977 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PASD1. The table records no clinical significance for this variant.

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Reference-table entries

PASD1Not classified

Variant type: synonymous_variant
HGVS: NM_173493.3,c.513A>G,p.Gly171Gly
Allele change: Synonymous_G171G

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.