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Variant (rsID / SNP)

rs1058642

NIPSNAP1

rs1058642 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NIPSNAP1. Location: chromosome 22, position 29,957,570. The table records no clinical significance for this variant.

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Reference-table entries

NIPSNAP1Not classified
Variant type
synonymous_variant
Chromosome / position
22:29957570
HGVS
NM_003634.4,c.504C>T,p.Leu168Leu
Allele change
Synonymous_L148L

Public references

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