Variant (rsID / SNP)

rs11211247

rs11211247 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MAST2. Location: chromosome 1, position 46,476,587. The table records no clinical significance for this variant.

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Reference-table entries

MAST2Not classified

Variant type: missense_variant
Chromosome / position: 1:46476587
HGVS: NM_001324320.2,c.1185T>G,p.Asp395Glu
Allele change: Missense_D395E

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.