Variant (rsID / SNP)

rs1132375

rs1132375 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANKLE2. Location: chromosome 12, position 133,331,537. The table records no clinical significance for this variant.

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Reference-table entries

ANKLE2Not classified

Variant type: missense_variant
Chromosome / position: 12:133331537
HGVS: NM_015114.3,c.364C>T,p.His122Tyr
Allele change: Missense_H122Y

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.