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Variant (rsID / SNP)

rs3130250

MOG

rs3130250 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MOG. Location: chromosome 6, position 29,625,001. The table records no clinical significance for this variant.

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Reference-table entries

MOGNot classified
Variant type
synonymous_variant
Chromosome / position
6:29625001
HGVS
NM_001363610.2,c.15A>G,p.Ser5Ser
Allele change
Synonymous_S5S

Associated conditions / phenotypes

Synonymous_S5S|Synonymous_S5S|Synonymous_S5S|Synonymous_S5S|Synonymous_S5S

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.