Variant (rsID / SNP)

rs11174557

rs11174557 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MON2. Location: chromosome 12, position 62,979,216. The table records no clinical significance for this variant.

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Reference-table entries

MON2Not classified

Variant type: synonymous_variant
Chromosome / position: 12:62979216
HGVS: NM_015026.3,c.4842G>A,p.Arg1614Arg
Allele change: Synonymous_R1614R

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.