Variant (rsID / SNP)

rs7698598

rs7698598 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SYNPO2. Location: chromosome 4, position 119,951,647. The table records no clinical significance for this variant.

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Reference-table entries

SYNPO2Not classified

Variant type: missense_variant
Chromosome / position: 4:119951647
HGVS: NM_133477.3,c.1717A>G,p.Thr573Ala
Allele change: Missense_T542A

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.