Variant (rsID / SNP)

rs35154152

rs35154152 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to THBS3. Location: chromosome 1, position 155,172,725. The table records no clinical significance for this variant.

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Reference-table entries

THBS3Not classified

Variant type: missense_variant
Chromosome / position: 1:155172725
HGVS: NM_007112.5,c.835A>G,p.Ser279Gly
Allele change: Missense_S159G

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.