Variant (rsID / SNP)

rs62489646

rs62489646 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ASB10. Location: chromosome 7, position 150,873,754. Clinical significance in the table: Benign.

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Reference-table entries

ASB10Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:150873754
Cytoband: 7q36.1
HGVS: NM_001142459.2(ASB10):c.1114C>T (p.Arg372Cys)
Allele change: Missense_R372C

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.