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Variant (rsID / SNP)

rs10839708

NLRP14

rs10839708 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NLRP14. Location: chromosome 11, position 7,079,038. The table records no clinical significance for this variant.

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Reference-table entries

NLRP14Not classified
Variant type
missense_variant
Chromosome / position
11:7079038
HGVS
NM_176822.4,c.2422G>A,p.Glu808Lys
Allele change
Missense_E808K

Public references

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