Variant (rsID / SNP)

rs281393

rs281393 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAMSTR, RASIP1. Location: chromosome 19, position 49,224,484. The table records no clinical significance for this variant.

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Reference-table entries

MAMSTRNot classified

Variant type: upstream_gene_variant
Chromosome / position: 19:49224484
HGVS: NM_001130915.2,c.-1570G>A
Allele change: Silent

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.