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Variant (rsID / SNP)

rs35142632

RIN2

rs35142632 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RIN2. Location: chromosome 20, position 19,956,096. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

RIN2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
20:19956096
Cytoband
20p11.23
HGVS
NM_018993.4(RIN2):c.1427C>G (p.Pro476Arg)
Allele change
Missense_P525R

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.