Variant (rsID / SNP)

rs17778003

rs17778003 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZFAT. Location: chromosome 8, position 135,669,810. The table records no clinical significance for this variant.

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Reference-table entries

ZFATNot classified

Variant type: missense_variant
Chromosome / position: 8:135669810
HGVS: NM_020863.4,c.190G>A,p.Gly64Arg
Allele change: Missense_G52R

Associated conditions / phenotypes

Missense_G52R|Missense_G52R

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.