Variant (rsID / SNP)

rs3744307

rs3744307 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC16A6. Location: chromosome 17, position 66,267,650. The table records no clinical significance for this variant.

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Reference-table entries

SLC16A6Not classified

Variant type: missense_variant
Chromosome / position: 17:66267650
HGVS: NM_001174166.2,c.651A>C,p.Glu217Asp
Allele change: Silent

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.