Variant (rsID / SNP)

rs148915050

rs148915050 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SOBP. Location: chromosome 6, position 107,827,529. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

SOBPBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 6:107827529
Cytoband: 6q21
HGVS: NM_018013.4(SOBP):c.319A>G (p.Thr107Ala)
Allele change: Missense_T107A

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.