Variant (rsID / SNP)

rs6926980

rs6926980 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIAA1586. Location: chromosome 6, position 56,917,538. The table records no clinical significance for this variant.

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Reference-table entries

KIAA1586Not classified

Variant type: missense_variant
Chromosome / position: 6:56917538
HGVS: NM_020931.4,c.241G>A,p.Val81Met
Allele change: Missense_V54M

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.