Variant (rsID / SNP)

rs3795504

rs3795504 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIAA1614. Location: chromosome 1, position 180,905,448. The table records no clinical significance for this variant.

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Reference-table entries

KIAA1614Not classified

Variant type: missense_variant
Chromosome / position: 1:180905448
HGVS: NM_020950.2,c.2403G>T,p.Leu801Phe
Allele change: Missense_L801F

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.