Variant (rsID / SNP)

rs1105385

rs1105385 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLHDC8A. Location: chromosome 1, position 205,308,335. The table records no clinical significance for this variant.

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Reference-table entries

KLHDC8ANot classified

Variant type: synonymous_variant
Chromosome / position: 1:205308335
HGVS: NM_001271863.2,c.744C>T,p.Phe248Phe
Allele change: Synonymous_F248F

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.