Variant (rsID / SNP)

rs12919

rs12919 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NOM1. Location: chromosome 7, position 156,762,248. The table records no clinical significance for this variant.

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Reference-table entries

NOM1Not classified

Variant type: missense_variant
Chromosome / position: 7:156762248
HGVS: NM_001353366.2,c.2437G>A,p.Val813Met
Allele change: Missense_V812M

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.