Variant (rsID / SNP)

rs2967951

rs2967951 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ROPN1L. Location: chromosome 5, position 10,464,107. The table records no clinical significance for this variant.

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Reference-table entries

ROPN1LNot classified

Variant type: intron_variant
Chromosome / position: 5:10464107
HGVS: NM_001201466.2,c.594-853C>T
Allele change: Silent

Associated conditions / phenotypes

Body Mass Index Quantitative Trait Locus 1

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.