Variant (rsID / SNP)

rs61741104

rs61741104 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SHROOM3. Location: chromosome 4, position 77,675,925. Clinical significance in the table: Benign.

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Reference-table entries

SHROOM3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:77675925
Cytoband: 4q21.1
HGVS: NM_020859.4(SHROOM3):c.4289G>A (p.Arg1430Gln)
Allele change: Missense_R1430Q

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.