Variant (rsID / SNP)

rs116772138

rs116772138 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FCHSD1. Location: chromosome 5, position 141,021,294. The table records no clinical significance for this variant.

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Reference-table entries

FCHSD1Not classified

Variant type: missense_variant
Chromosome / position: 5:141021294
HGVS: NM_033449.3,c.1982A>C,p.Asp661Ala
Allele change: Missense_D661A

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.