Variant (rsID / SNP)

rs62621812

rs62621812 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZNF800. Location: chromosome 7, position 127,015,083. The table records no clinical significance for this variant.

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Reference-table entries

ZNF800Not classified

Variant type: missense_variant
Chromosome / position: 7:127015083
HGVS: NM_176814.5,c.307C>T,p.Pro103Ser
Allele change: Missense_P103S

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.