Variant (rsID / SNP)

rs760998

rs760998 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIAA1755. Location: chromosome 20, position 36,845,738. The table records no clinical significance for this variant.

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Reference-table entries

KIAA1755Not classified

Variant type: missense_variant
Chromosome / position: 20:36845738
HGVS: NM_001029864.2,c.2818G>A,p.Glu940Lys
Allele change: Missense_E940K

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.