Variant (rsID / SNP)

rs17549193

rs17549193 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FCN2. Location: chromosome 9, position 137,779,026. The table records no clinical significance for this variant.

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Reference-table entries

FCN2Not classified

Variant type: missense_variant
Chromosome / position: 9:137779026
HGVS: NM_004108.3,c.707C>T,p.Thr236Met
Allele change: Missense_T236M

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.