Variant (rsID / SNP)

rs2270927

rs2270927 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SV2C. Location: chromosome 5, position 75,591,710. The table records no clinical significance for this variant.

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Reference-table entries

SV2CNot classified

Variant type: missense_variant
Chromosome / position: 5:75591710
HGVS: NM_014979.4,c.1445C>G,p.Thr482Ser
Allele change: Missense_T482S

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.