Variant (rsID / SNP)

rs1043149

rs1043149 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZACN, EXOC7. Location: chromosome 17, position 74,077,797. The table records no clinical significance for this variant.

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Reference-table entries

ZACNNot classified

Variant type: stop_gained
Chromosome / position: 17:74077797
HGVS: NM_180990.4,c.841C>T,p.Gln281*
Allele change: Nonsense_Q281X

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.