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Variant (rsID / SNP)

rs2273431

NID2

rs2273431 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NID2. Location: chromosome 14, position 52,496,407. The table records no clinical significance for this variant.

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Reference-table entries

NID2Not classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
14:52496407
HGVS
NM_007361.4,c.2259G>A,p.Glu753Glu
Allele change
Synonymous_E753E

Public references

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