Variant (rsID / SNP)

rs78648341

rs78648341 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RIN2. Location: chromosome 20, position 19,915,770. 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: 20:19915770
Cytoband: 20p11.23
HGVS: NM_018993.4(RIN2):c.85G>A (p.Gly29Arg)
Allele change: Missense_G78R

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.