Variant (rsID / SNP)

rs113947297

rs113947297 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RINT1. Location: chromosome 7, position 105,188,996. Clinical significance in the table: Benign.

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Reference-table entries

RINT1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:105188996
Cytoband: 7q22.3
HGVS: NM_021930.6(RINT1):c.840-5G>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.