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Variant (rsID / SNP)

rs12130792

OLFML2B

rs12130792 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OLFML2B. Location: chromosome 1, position 161,993,192. The table records no clinical significance for this variant.

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Reference-table entries

OLFML2BNot classified
Variant type
missense_variant
Chromosome / position
1:161993192
HGVS
NM_001347700.2,c.29A>G,p.Tyr10Cys
Allele change
Missense_Y10C

Public references

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