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Variant (rsID / SNP)

rs10742156

SLC5A12

rs10742156 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC5A12. Location: chromosome 11, position 26,734,209. The table records no clinical significance for this variant.

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Reference-table entries

SLC5A12Not classified
Variant type
synonymous_variant
Chromosome / position
11:26734209
HGVS
NM_178498.4,c.384G>A,p.Thr128Thr
Allele change
Synonymous_T128T

Public references

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