Variant (rsID / SNP)

rs11576830

rs11576830 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KLHDC9. Location: chromosome 1, position 161,068,836. The table records no clinical significance for this variant.

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Reference-table entries

KLHDC9Not classified

Variant type: missense_variant
Chromosome / position: 1:161068836
HGVS: NM_152366.5,c.511A>C,p.Ser171Arg
Allele change: Silent

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.