Variant (rsID / SNP)

rs2270976

rs2270976 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARHGEF10L. Location: chromosome 1, position 18,023,690. The table records no clinical significance for this variant.

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Reference-table entries

ARHGEF10LNot classified

Variant type: missense_variant
Chromosome / position: 1:18023690
HGVS: NM_018125.4,c.3655A>G,p.Ile1219Val
Allele change: Missense_I1219V

Associated conditions / phenotypes

Missense_I922V

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.