Variant (rsID / SNP)

rs61753649

rs61753649 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FHDC1. Location: chromosome 4, position 153,874,666. The table records no clinical significance for this variant.

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Reference-table entries

FHDC1Not classified

Variant type: missense_variant
Chromosome / position: 4:153874666
HGVS: NM_001371116.1,c.514G>A,p.Ala172Thr
Allele change: Missense_A172T

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.