Variant (rsID / SNP)

rs111418068

rs111418068 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIRREL3. Location: chromosome 11, position 126,343,227. Clinical significance in the table: Likely benign.

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Reference-table entries

KIRREL3Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 11:126343227
Cytoband: 11q24.2
HGVS: NM_032531.4(KIRREL3):c.568A>G (p.Ile190Val)
Allele change: Missense_I190V

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.