Variant (rsID / SNP)

rs2070097

rs2070097 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARHGAP4. Clinical significance in the table: Benign.

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Reference-table entries

ARHGAP4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xq28
HGVS: NM_001666.5(ARHGAP4):c.1716T>C (p.His572=)
Allele change: Synonymous_H572H

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.