Variant (rsID / SNP)

rs3750823

rs3750823 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MMRN2, SNCG. Location: chromosome 10, position 88,717,154. The table records no clinical significance for this variant.

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Reference-table entries

MMRN2Not classified

Variant type: missense_variant
Chromosome / position: 10:88717154
HGVS: NM_024756.3,c.145G>A,p.Gly49Ser
Allele change: Missense_G49S

Associated conditions / phenotypes

Parkinson Disease, Late-Onset

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.