Variant (rsID / SNP)

rs117048984

rs117048984 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF467, SSPOP. Location: chromosome 7, position 149,473,614. The table records no clinical significance for this variant.

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Reference-table entries

ZNF467Not classified

Variant type: upstream_gene_variant
Chromosome / position: 7:149473614
HGVS: NM_207336.3,c.-3460T>C
Allele change: Missense_Y77C

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.