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Variant (rsID / SNP)

rs35039245

SH3BP4

rs35039245 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SH3BP4. Location: chromosome 2, position 235,950,391. The table records no clinical significance for this variant.

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Reference-table entries

SH3BP4Not classified
Variant type
synonymous_variant
Chromosome / position
2:235950391
HGVS
NM_001371302.1,c.978C>T,p.Ser326Ser
Allele change
Synonymous_S326S

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.