Variant (rsID / SNP)

rs61755995

rs61755995 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NIN. Location: chromosome 14, position 51,219,349. Clinical significance in the table: Benign.

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Reference-table entries

NINBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 14:51219349
Cytoband: 14q22.1
HGVS: NM_020921.4(NIN):c.4837C>T (p.Arg1613Cys)
Allele change: Missense_R1613C

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.