Variant (rsID / SNP)

rs17094900

rs17094900 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRRIQ3. Location: chromosome 1, position 74,648,408. The table records no clinical significance for this variant.

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Reference-table entries

LRRIQ3Not classified

Variant type: missense_variant
Chromosome / position: 1:74648408
HGVS: NM_001105659.2,c.387G>A,p.Met129Ile
Allele change: Missense_M129I

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.