Variant (rsID / SNP)

rs35997283

rs35997283 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRIT3. Location: chromosome 4, position 110,791,526. Clinical significance in the table: Likely benign.

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Reference-table entries

LRIT3Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 4:110791526
Cytoband: 4q25
HGVS: NM_198506.5(LRIT3):c.1621A>G (p.Ile541Val)
Allele change: Missense_I541V

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.