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Variant (rsID / SNP)

rs7913176

NHLRC2

rs7913176 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NHLRC2. Location: chromosome 10, position 115,644,040. The table records no clinical significance for this variant.

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Reference-table entries

NHLRC2Not classified
Variant type
missense_variant
Chromosome / position
10:115644040
HGVS
NM_198514.4,c.940G>A,p.Val314Ile
Allele change
Missense_V314I

Public references

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