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Variant (rsID / SNP)

rs35996697

ANKMY1

rs35996697 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANKMY1. Location: chromosome 2, position 241,463,595. The table records no clinical significance for this variant.

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Reference-table entries

ANKMY1Not classified
Variant type
missense_variant
Chromosome / position
2:241463595
HGVS
NM_001282771.3,c.1539A>G,p.Ile513Met
Allele change
Missense_I362M

Associated conditions / phenotypes

Missense_I513M|Missense_I513M|Missense_I424M|Missense_I283M|Missense_I283M|Silent|Missense_I194M

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.