Variant (rsID / SNP)

rs35899692

rs35899692 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAF7L. The table records no clinical significance for this variant.

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Reference-table entries

TAF7LNot classified

Variant type: missense_variant
HGVS: NM_024885.4,c.922A>G,p.Ser308Gly
Allele change: Missense_S222G

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.