Variant (rsID / SNP)

rs34552277

rs34552277 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANKRD30A. Location: chromosome 10, position 37,505,159. The table records no clinical significance for this variant.

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Reference-table entries

ANKRD30ANot classified

Variant type: missense_variant
Chromosome / position: 10:37505159
HGVS: NM_052997.3,c.2920G>A,p.Ala974Thr
Allele change: Missense_A918T

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.