Variant (rsID / SNP)

rs41306763

rs41306763 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RIN2. Location: chromosome 20, position 19,955,473. Clinical significance in the table: Benign.

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Reference-table entries

RIN2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 20:19955473
Cytoband: 20p11.23
HGVS: NM_018993.4(RIN2):c.804C>T (p.Ala268=)
Allele change: Synonymous_A317A

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.