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Variant (rsID / SNP)

rs191837710

OBSCN

rs191837710 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OBSCN. Location: chromosome 1, position 228,399,519. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

OBSCNConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
1:228399519
Cytoband
1q42.13
HGVS
NM_001386125.1(OBSCN):c.35T>A (p.Phe12Tyr)
Allele change
Silent

Public references

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