Variant (rsID / SNP)

rs11722476

rs11722476 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SMARCAD1. Location: chromosome 4, position 95,170,839. The table records no clinical significance for this variant.

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Reference-table entries

SMARCAD1Not classified

Variant type: missense_variant
Chromosome / position: 4:95170839
HGVS: NM_001128429.3,c.740G>A,p.Ser247Asn
Allele change: Missense_S247N

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.