Variant (rsID / SNP)

rs676314

rs676314 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NAPSA. Location: chromosome 19, position 50,865,535. The table records no clinical significance for this variant.

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Reference-table entries

NAPSANot classified

Variant type: missense_variant
Chromosome / position: 19:50865535
HGVS: NM_004851.3,c.119T>C,p.Ile40Thr
Allele change: Missense_I40T

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.