Variant (rsID / SNP)

rs3763980

rs3763980 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC16A7. Location: chromosome 12, position 60,173,356. The table records no clinical significance for this variant.

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Reference-table entries

SLC16A7Not classified

Variant type: missense_variant
Chromosome / position: 12:60173356
HGVS: NM_001270622.2,c.1333A>T,p.Thr445Ser
Allele change: Missense_T445S

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.