Variant (rsID / SNP)

rs201092215

rs201092215 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AMER1. Location: chromosome X, position 63,410,516. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

AMER1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: X:63410516
Cytoband: Xq11.2
HGVS: NM_152424.4(AMER1):c.2651C>T (p.Pro884Leu)
Allele change: Missense_P884L

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.