Variant (rsID / SNP)

rs7094132

rs7094132 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WAPL. Location: chromosome 10, position 88,203,068. The table records no clinical significance for this variant.

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Reference-table entries

WAPLNot classified

Variant type: synonymous_variant
Chromosome / position: 10:88203068
HGVS: NM_015045.5,c.3375A>G,p.Thr1125Thr
Allele change: Synonymous_T1119T

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.