Variant (rsID / SNP)

rs201927115

rs201927115 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARHGAP31. Location: chromosome 3, position 119,101,142. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ARHGAP31Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 3:119101142
Cytoband: 3q13.33
HGVS: NM_020754.4(ARHGAP31):c.435C>G (p.Thr145=)
Allele change: Synonymous_T145T

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.