Variant (rsID / SNP)

rs11568952

rs11568952 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to EGF. Location: chromosome 4, position 110,884,319. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

EGFBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 4:110884319
Cytoband: 4q25
HGVS: NM_001963.6(EGF):c.1313-10G>T
Allele change: Silent

Associated conditions / phenotypes

Renal hypomagnesemia 4

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.