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Variant (rsID / SNP)

rs514024

SH2D3C

rs514024 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SH2D3C. Location: chromosome 9, position 130,504,070. The table records no clinical significance for this variant.

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Reference-table entries

SH2D3CNot classified
Variant type
synonymous_variant
Chromosome / position
9:130504070
HGVS
NM_170600.3,c.2085C>T,p.Ala695Ala
Allele change
Synonymous_A535A

Associated conditions / phenotypes

Synonymous_A695A|Synonymous_A627A

Public references

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