Variant (rsID / SNP)

rs61751925

rs61751925 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARSH. Clinical significance in the table: Benign.

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Reference-table entries

ARSHBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xp22.33
HGVS: NM_001011719.2(ARSH):c.1160C>T (p.Thr387Met)
Allele change: Missense_T387M

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.