Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs1402467

SULT1C4

rs1402467 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SULT1C4. Location: chromosome 2, position 108,994,808. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

SULT1C4Not classified
Variant type
missense_variant
Chromosome / position
2:108994808
HGVS
NM_006588.4,c.15C>G,p.Asp5Glu
Allele change
Silent

Public references

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