Variant (rsID / SNP)

rs3108171

rs3108171 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF382. Location: chromosome 19, position 37,117,302. The table records no clinical significance for this variant.

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Reference-table entries

ZNF382Not classified

Variant type: missense_variant
Chromosome / position: 19:37117302
HGVS: NM_001398490.1,c.503A>G,p.Glu168Gly
Allele change: Missense_E168G

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.