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Variant (rsID / SNP)

rs7191331

SLC38A7

rs7191331 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC38A7. Location: chromosome 16, position 58,713,798. The table records no clinical significance for this variant.

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Reference-table entries

SLC38A7Not classified
Variant type
missense_variant
Chromosome / position
16:58713798
HGVS
NM_001369608.1,c.233C>T,p.Thr78Ile
Allele change
Missense_T78I

Public references

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