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Variant (rsID / SNP)

rs3130253

MOG

rs3130253 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MOG. Location: chromosome 6, position 29,634,012. The table records no clinical significance for this variant.

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Reference-table entries

MOGNot classified
Variant type
missense_variant
Chromosome / position
6:29634012
HGVS
NM_001363610.2,c.520A>G,p.Ile174Val
Allele change
Missense_I174V

Associated conditions / phenotypes

Autoimmune Disease|Multiple Sclerosis|Missense_I174V|Missense_I174V|Missense_I58V

Public references

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