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Variant (rsID / SNP)

rs3800544

WDR27

rs3800544 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR27. Location: chromosome 6, position 170,058,374. The table records no clinical significance for this variant.

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Reference-table entries

WDR27Not classified
Variant type
missense_variant&splice_region_variant
Chromosome / position
6:170058374
HGVS
NM_182552.5,c.1400G>A,p.Arg467His
Allele change
Missense_R467H

Associated conditions / phenotypes

Silent|Missense_R399H

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.