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Variant (rsID / SNP)

rs115476782

BTNL10

rs115476782 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BTNL10. Location: chromosome 1, position 228,698,311. The table records no clinical significance for this variant.

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Reference-table entries

BTNL10Not classified
Variant type
non_coding_transcript_exon_variant
Chromosome / position
1:228698311
HGVS
NR_172558.1,n.880G>T
Allele change
Missense_A126S

Public references

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