Variant (rsID / SNP)

rs111393448

rs111393448 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPOCK1. Location: chromosome 5, position 136,834,138. Clinical significance in the table: Benign.

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Reference-table entries

SPOCK1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:136834138
Cytoband: 5q31.2
HGVS: NM_004598.4(SPOCK1):c.110A>G (p.Asn37Ser)
Allele change: Missense_N37S

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.