Variant (rsID / SNP)

rs77871693

rs77871693 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SULF1. Location: chromosome 8, position 70,571,035. The table records no clinical significance for this variant.

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Reference-table entries

SULF1Not classified

Variant type: 3_prime_UTR_variant
Chromosome / position: 8:70571035
HGVS: NM_001128204.2,c.*265C>T
Allele change: Silent

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.