Variant (rsID / SNP)

rs842192

rs842192 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SEC16B. Location: chromosome 1, position 177,915,474. The table records no clinical significance for this variant.

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Reference-table entries

SEC16BNot classified

Variant type: missense_variant
Chromosome / position: 1:177915474
HGVS: NM_001356499.2,c.1859T>G,p.Ile620Ser
Allele change: Silent

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.