Variant (rsID / SNP)

rs62621834

rs62621834 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OBSCN. Location: chromosome 1, position 228,480,317. Clinical significance in the table: Benign.

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Reference-table entries

OBSCNBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:228480317
Cytoband: 1q42.13
HGVS: NM_001386125.1(OBSCN):c.11984C>T (p.Pro3995Leu)
Allele change: Missense_P3995L

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.