Variant (rsID / SNP)

rs10100659

rs10100659 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TGS1. Location: chromosome 8, position 56,708,701. The table records no clinical significance for this variant.

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Reference-table entries

TGS1Not classified

Variant type: missense_variant
Chromosome / position: 8:56708701
HGVS: NM_024831.8,c.1532T>C,p.Ile511Thr
Allele change: Missense_I418T

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.