Variant (rsID / SNP)

rs6795577

rs6795577 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SSUH2. Location: chromosome 3, position 8,693,750. The table records no clinical significance for this variant.

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Reference-table entries

SSUH2Not classified

Variant type: 5_prime_UTR_premature_start_codon_gain_variant
Chromosome / position: 3:8693750
HGVS: NM_001256749.3,c.-266C>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.