Variant (rsID / SNP)

rs11559146

rs11559146 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZDHHC4. Location: chromosome 7, position 6,621,277. The table records no clinical significance for this variant.

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Reference-table entries

ZDHHC4Not classified

Variant type: missense_variant
Chromosome / position: 7:6621277
HGVS: NM_001371292.1,c.157G>A,p.Val53Met
Allele change: Missense_V53M

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.