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Variant (rsID / SNP)

rs13014235

FLACC1

rs13014235 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLACC1. Location: chromosome 2, position 202,215,492. The table records no clinical significance for this variant.

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Reference-table entries

FLACC1Not classified
Variant type
missense_variant
Chromosome / position
2:202215492
HGVS
NM_139163.4,c.127G>C,p.Val43Leu
Allele change
Missense_V43L

Associated conditions / phenotypes

Basal Cell Carcinoma

Public references

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