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Variant (rsID / SNP)

rs12375547

WDR38

rs12375547 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WDR38. Location: chromosome 9, position 127,616,537. The table records no clinical significance for this variant.

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Reference-table entries

WDR38Not classified
Variant type
missense_variant
Chromosome / position
9:127616537
HGVS
NM_001276376.2,c.29A>G,p.Lys10Arg
Allele change
Synonymous_E41E

Public references

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