Variant (rsID / SNP)

rs10899918

rs10899918 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NA, LOC107984189. Location: chromosome 10, position 44,321,351. The table records no clinical significance for this variant.

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Reference-table entries

NANot classified

Variant type: intergenic_region
Chromosome / position: 10:44321351
HGVS: NA,n.44321351T>G

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.