Variant (rsID / SNP)

rs671694

rs671694 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SDK1. Location: chromosome 7, position 4,213,975. The table records no clinical significance for this variant.

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Reference-table entries

SDK1Not classified

Variant type: missense_variant
Chromosome / position: 7:4213975
HGVS: NM_152744.4,c.4922A>G,p.His1641Arg
Allele change: Missense_H1641R

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.