Variant (rsID / SNP)

rs121908601

rs121908601 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZFPM2. Location: chromosome 8, position 106,431,420. Clinical significance in the table: Likely benign.

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Reference-table entries

ZFPM2Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 8:106431420
Cytoband: 8q23.1
HGVS: NM_012082.4(ZFPM2):c.89A>G (p.Glu30Gly)
Allele change: Silent

Associated conditions / phenotypes

Tetralogy of Fallot|Double outlet right ventricle|Diaphragmatic hernia 3|46,XY sex reversal 9|46,XY sex reversal 3

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.