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Variant (rsID / SNP)

rs2302837

WSCD1

rs2302837 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WSCD1. Location: chromosome 17, position 6,014,176. The table records no clinical significance for this variant.

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Reference-table entries

WSCD1Not classified
Variant type
synonymous_variant
Chromosome / position
17:6014176
HGVS
NM_001388405.1,c.1095A>G,p.Thr365Thr
Allele change
Synonymous_T365T

Public references

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