Variant (rsID / SNP)

rs1771487

rs1771487 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OBSCN. Location: chromosome 1, position 228,402,121. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

OBSCNNot classified

Variant type: missense_variant
Chromosome / position: 1:228402121
HGVS: NM_001386125.1,c.1505A>G,p.Gln502Arg
Allele change: Missense_Q502R

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.