Variant (rsID / SNP)

rs75449932

rs75449932 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIF14. Location: chromosome 1, position 200,534,651. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

KIF14Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 1:200534651
Cytoband: 1q32.1
HGVS: NM_014875.3(KIF14):c.3808A>C (p.Ser1270Arg)
Allele change: Missense_S1270R

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.