Variant (rsID / SNP)

rs3779721

rs3779721 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NIPAL2. Location: chromosome 8, position 99,208,190. The table records no clinical significance for this variant.

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Reference-table entries

NIPAL2Not classified

Variant type: synonymous_variant
Chromosome / position: 8:99208190
HGVS: NM_001321635.2,c.924T>G,p.Thr308Thr
Allele change: Synonymous_T308T

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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