Variant (rsID / SNP)

rs3013105

rs3013105 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRRC38. Location: chromosome 1, position 13,802,325. The table records no clinical significance for this variant.

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Reference-table entries

LRRC38Not classified

Variant type: missense_variant
Chromosome / position: 1:13802325
HGVS: NM_001010847.2,c.874A>G,p.Lys292Glu
Allele change: Missense_K292E

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.