Variant (rsID / SNP)

rs35667623

rs35667623 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WHAMM. Location: chromosome 15, position 83,486,700. Clinical significance in the table: Benign.

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Reference-table entries

WHAMMBenign

Clinical significance (as recorded): Benign
Variant type: synonymous_variant
Chromosome / position: 15:83486700
HGVS: NM_001080435.3,c.963G>A,p.Ala321Ala
Allele change: Synonymous_A321A

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.