Variant (rsID / SNP)

rs11146963

rs11146963 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRCOL1. Location: chromosome 12, position 133,181,399. The table records no clinical significance for this variant.

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Reference-table entries

LRCOL1Not classified

Variant type: missense_variant
Chromosome / position: 12:133181399
HGVS: NM_001195520.2,c.124A>G,p.Arg42Gly
Allele change: Missense_R42G

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.