Variant (rsID / SNP)

rs2400891

rs2400891 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARHGEF37. Location: chromosome 5, position 148,989,122. The table records no clinical significance for this variant.

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Reference-table entries

ARHGEF37Not classified

Variant type: synonymous_variant
Chromosome / position: 5:148989122
HGVS: NM_001001669.3,c.322C>T,p.Leu108Leu
Allele change: Synonymous_L108L

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.