Variant (rsID / SNP)

rs41265385

rs41265385 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR27. Location: chromosome 6, position 170,068,086. The table records no clinical significance for this variant.

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Reference-table entries

WDR27Not classified

Variant type: missense_variant
Chromosome / position: 6:170068086
HGVS: NM_182552.5,c.652G>A,p.Gly218Ser
Allele change: Missense_G218S

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.