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Variant (rsID / SNP)

rs61748682

SYNJ2

rs61748682 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SYNJ2. Location: chromosome 6, position 158,487,570. The table records no clinical significance for this variant.

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Reference-table entries

SYNJ2Not classified
Variant type
synonymous_variant
Chromosome / position
6:158487570
HGVS
NM_003898.4,c.1620C>T,p.Asn540Asn
Allele change
Synonymous_N540N

Public references

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