Variant (rsID / SNP)

rs6017667

rs6017667 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPINT4, WFDC3. Location: chromosome 20, position 44,352,620. The table records no clinical significance for this variant.

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Reference-table entries

SPINT4Not classified

Variant type: missense_variant
Chromosome / position: 20:44352620
HGVS: NM_178455.3,c.217G>A,p.Gly73Ser
Allele change: Missense_G73S

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.