Variant (rsID / SNP)

rs3750399

rs3750399 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SHC3. Location: chromosome 9, position 91,656,963. The table records no clinical significance for this variant.

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Reference-table entries

SHC3Not classified

Variant type: synonymous_variant
Chromosome / position: 9:91656963
HGVS: NM_016848.6,c.1338A>G,p.Pro446Pro
Allele change: Synonymous_P446P

Associated conditions / phenotypes

Smoking As a Quantitative Trait Locus 3|Tobacco Addiction

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.