Variant (rsID / SNP)

rs34973107

rs34973107 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ELMOD3. Location: chromosome 2, position 85,617,310. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ELMOD3Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 2:85617310
Cytoband: 2p11.2
HGVS: NM_001135022.2(ELMOD3):c.865G>A (p.Ala289Thr)
Allele change: Missense_A289T

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.