Variant (rsID / SNP)

rs13342692

rs13342692 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC16A11. Location: chromosome 17, position 6,946,287. The table records no clinical significance for this variant.

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Reference-table entries

SLC16A11Not classified

Variant type: missense_variant
Chromosome / position: 17:6946287
HGVS: NM_001370549.1,c.308A>G,p.Asp103Gly
Allele change: Missense_D127G

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.