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Variant (rsID / SNP)

rs34976233

KLHDC7A

rs34976233 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLHDC7A. Location: chromosome 1, position 18,807,755. The table records no clinical significance for this variant.

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Reference-table entries

KLHDC7ANot classified
Variant type
missense_variant
Chromosome / position
1:18807755
HGVS
NM_152375.3,c.280G>A,p.Gly94Ser
Allele change
Missense_G94S

Public references

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