Variant (rsID / SNP)

rs11099273

rs11099273 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PABPC4L. Location: chromosome 4, position 135,121,066. The table records no clinical significance for this variant.

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Reference-table entries

PABPC4LNot classified

Variant type: missense_variant
Chromosome / position: 4:135121066
HGVS: NM_001114734.2,c.1109A>C,p.His370Pro
Allele change: Missense_H370P

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.