Variant (rsID / SNP)

rs4698797

rs4698797 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRIT3. Location: chromosome 4, position 110,773,067. Clinical significance in the table: Benign.

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Reference-table entries

LRIT3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:110773067
Cytoband: 4q25
HGVS: NM_198506.5(LRIT3):c.524G>A (p.Ser175Asn)
Allele change: Missense_S175N

Associated conditions / phenotypes

Congenital Stationary Night Blindness, Recessive|Congenital stationary night blindness 1F

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.