Variant (rsID / SNP)

rs139111924

rs139111924 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPR101. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

GPR101Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Cytoband: Xq26.3
HGVS: NM_054021.2(GPR101):c.712G>A (p.Val238Ile)
Allele change: Missense_V238I

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.