Variant (rsID / SNP)

rs3747495

rs3747495 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC180, SUGT1P4-STRA6LP-CCDC180. Location: chromosome 9, position 100,122,291. The table records no clinical significance for this variant.

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Reference-table entries

CCDC180Not classified

Variant type: missense_variant
Chromosome / position: 9:100122291
HGVS: NM_020893.6,c.3391T>C,p.Phe1131Leu
Allele change: Silent

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.