Variant (rsID / SNP)

rs7076156

rs7076156 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF365, LOC105378327. Location: chromosome 10, position 64,415,184. Clinical significance in the table: Benign.

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Reference-table entries

ZNF365Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:64415184
Cytoband: 10q21.2
HGVS: NM_199451.3(ZNF365):c.1130-972=
Allele change: Silent

Associated conditions / phenotypes

Nephrolithiasis, uric acid, susceptibility to

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.