Variant (rsID / SNP)

rs7271

rs7271 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC61. Location: chromosome 19, position 46,518,682. The table records no clinical significance for this variant.

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Reference-table entries

CCDC61Not classified

Variant type: missense_variant
Chromosome / position: 19:46518682
HGVS: NM_001267723.2,c.842G>A,p.Arg281Lys
Allele change: Missense_R281K

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.