Variant (rsID / SNP)

rs1493953

rs1493953 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MICAL2, MICALCL. Location: chromosome 11, position 12,315,891. The table records no clinical significance for this variant.

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Reference-table entries

MICAL2Not classified

Variant type: missense_variant
Chromosome / position: 11:12315891
HGVS: NM_001393937.1,c.4699G>A,p.Ala1567Thr
Allele change: Missense_A305T

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.