Variant (rsID / SNP)

rs3812754

rs3812754 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MICAL2, MICALCL. Location: chromosome 11, position 12,316,389. The table records no clinical significance for this variant.

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Reference-table entries

MICAL2Not classified

Variant type: missense_variant
Chromosome / position: 11:12316389
HGVS: NM_001393937.1,c.5197A>C,p.Thr1733Pro
Allele change: Missense_T471P

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.