Variant (rsID / SNP)

rs957448

rs957448 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VIRMA. Location: chromosome 8, position 95,541,302. The table records no clinical significance for this variant.

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Reference-table entries

VIRMANot classified

Variant type: synonymous_variant
Chromosome / position: 8:95541302
HGVS: NM_015496.5,c.876T>C,p.Gly292Gly
Allele change: Synonymous_G292G

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.