Variant (rsID / SNP)

rs114609276

rs114609276 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CFAP210, CCDC173. Location: chromosome 2, position 170,502,415. The table records no clinical significance for this variant.

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Reference-table entries

CFAP210Not classified

Variant type: missense_variant
Chromosome / position: 2:170502415
HGVS: NM_001085447.2,c.1595A>G,p.Tyr532Cys
Allele change: Missense_Y532C

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.