Variant (rsID / SNP)

rs1972977

rs1972977 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AADACL2, MIR548H2. Location: chromosome 3, position 151,463,421. The table records no clinical significance for this variant.

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Reference-table entries

AADACL2Not classified

Variant type: missense_variant
Chromosome / position: 3:151463421
HGVS: NM_207365.4,c.556G>T,p.Ala186Ser
Allele change: Silent

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.