Variant (rsID / SNP)

rs671756

rs671756 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SDK1. Location: chromosome 7, position 4,213,940. The table records no clinical significance for this variant.

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Reference-table entries

SDK1Not classified

Variant type: synonymous_variant
Chromosome / position: 7:4213940
HGVS: NM_152744.4,c.4887T>C,p.Thr1629Thr
Allele change: Synonymous_T1629T

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.