Variant (rsID / SNP)

rs3735319

rs3735319 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF777. Location: chromosome 7, position 149,152,770. The table records no clinical significance for this variant.

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Reference-table entries

ZNF777Not classified

Variant type: missense_variant
Chromosome / position: 7:149152770
HGVS: NM_015694.3,c.344T>C,p.Val115Ala
Allele change: Missense_V115A

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.