Variant (rsID / SNP)

rs191137

rs191137 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZAN. Location: chromosome 7, position 100,386,900. The table records no clinical significance for this variant.

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Reference-table entries

ZANNot classified

Variant type: missense_variant
Chromosome / position: 7:100386900
HGVS: NM_003386.3,c.7285T>C,p.Trp2429Arg
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.