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Variant (rsID / SNP)

rs10925061

OR2W5P

rs10925061 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR2W5P. Location: chromosome 1, position 247,654,993. The table records no clinical significance for this variant.

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Reference-table entries

OR2W5PNot classified
Variant type
non_coding_transcript_exon_variant
Chromosome / position
1:247654993
HGVS
NR_169841.1,n.873T>C
Allele change
Synonymous_S188S

Public references

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