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Variant (rsID / SNP)

rs2076523

BTNL2

rs2076523 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BTNL2. Location: chromosome 6, position 32,370,835. The table records no clinical significance for this variant.

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Reference-table entries

BTNL2Not classified
Variant type
missense_variant
Chromosome / position
6:32370835
HGVS
NM_001304561.2,c.586A>G,p.Lys196Glu
Allele change
Silent

Associated conditions / phenotypes

Colitis|Sarcoidosis 1|Ulcerative Colitis

Public references

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