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Variant (rsID / SNP)

rs33932952

SLC37A2

rs33932952 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC37A2. Location: chromosome 11, position 124,949,044. The table records no clinical significance for this variant.

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Reference-table entries

SLC37A2Not classified
Variant type
synonymous_variant
Chromosome / position
11:124949044
HGVS
NM_198277.3,c.351C>T,p.Tyr117Tyr
Allele change
Synonymous_Y117Y

Public references

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