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Variant (rsID / SNP)

rs16898671

KLHL38

rs16898671 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLHL38. Location: chromosome 8, position 124,658,210. The table records no clinical significance for this variant.

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Reference-table entries

KLHL38Not classified
Variant type
synonymous_variant
Chromosome / position
8:124658210
HGVS
NM_001081675.3,c.1515G>A,p.Ala505Ala
Allele change
Synonymous_A505A

Public references

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