Variant (rsID / SNP)

rs13075089

rs13075089 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GMNC. Location: chromosome 3, position 190,578,566. The table records no clinical significance for this variant.

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Reference-table entries

GMNCNot classified

Variant type: missense_variant
Chromosome / position: 3:190578566
HGVS: NM_001146686.3,c.85T>C,p.Ser29Pro
Allele change: Missense_S29P

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.