Variant (rsID / SNP)

rs114077715

rs114077715 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBLIM1. Location: chromosome 1, position 16,101,332. The table records no clinical significance for this variant.

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Reference-table entries

FBLIM1Not classified

Variant type: missense_variant
Chromosome / position: 1:16101332
HGVS: NM_001024215.1,c.931G>A,p.Gly311Arg
Allele change: Silent

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.