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Variant (rsID / SNP)

rs139566867

FBRSL1

rs139566867 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBRSL1. Location: chromosome 12, position 133,146,805. The table records no clinical significance for this variant.

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Reference-table entries

FBRSL1Not classified
Variant type
missense_variant
Chromosome / position
12:133146805
HGVS
NM_001142641.2,c.985G>A,p.Ala329Thr
Allele change
Missense_A329T

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.