Variant (rsID / SNP)

rs79073889

rs79073889 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANKS6. Location: chromosome 9, position 101,546,410. Clinical significance in the table: Benign.

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Reference-table entries

ANKS6Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 9:101546410
Cytoband: 9q22.33
HGVS: NM_173551.5(ANKS6):c.937G>A (p.Asp313Asn)
Allele change: Missense_D313N

Associated conditions / phenotypes

Nephronophthisis 16

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.