Variant (rsID / SNP)

rs147797700

rs147797700 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SZT2. Location: chromosome 1, position 43,897,496. Clinical significance in the table: Benign.

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Reference-table entries

SZT2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:43897496
Cytoband: 1p34.2
HGVS: NM_001365999.1(SZT2):c.5198G>A (p.Arg1733His)
Allele change: Missense_R1676H

Associated conditions / phenotypes

Seizure

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.