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Variant (rsID / SNP)

rs2294015

ANXA13

rs2294015 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANXA13. Location: chromosome 8, position 124,696,867. The table records no clinical significance for this variant.

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Reference-table entries

ANXA13Not classified
Variant type
missense_variant
Chromosome / position
8:124696867
HGVS
NM_001003954.3,c.937G>A,p.Val313Ile
Allele change
Missense_V272I

Public references

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