Variant (rsID / SNP)

rs4698775

rs4698775 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CASP6, MCUB. Location: chromosome 4, position 110,590,479. The table records no clinical significance for this variant.

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Reference-table entries

CASP6Not classified

Variant type: single nucleotide variant
Chromosome / position: 4:110590479
Cytoband: 4q25
HGVS: NM_017918.5(MCUB):c.451+4929G>T
Allele change: Silent

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.