Variant (rsID / SNP)

rs201414754

rs201414754 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SIN3A. Location: chromosome 15, position 75,688,804. Clinical significance in the table: Uncertain significance.

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Reference-table entries

SIN3AUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 15:75688804
Cytoband: 15q24.2
HGVS: NM_001145358.2(SIN3A):c.1888A>G (p.Ile630Val)
Allele change: Missense_I630V

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.