| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ARHGEF19, LOC129929521 (S299N) | Single nucleotide variant (missense variant) | not specified | |
| | ARHGEF19, LOC129929521 (S338N) | Single nucleotide variant (missense variant) | not specified | |
| | ARHGEF19, LOC129929521 (S336T) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | ARHGEF19, LOC129929521 (V366I) | Single nucleotide variant (missense variant) | not specified | |
| | ARHGEF19, LOC129929521 (I358T) | Single nucleotide variant (missense variant) | not specified | |
| | ARHGEF19, LOC129929521 (D374A) | Single nucleotide variant (missense variant) | not specified | |
| | ARHGEF19, LOC129929521 (R332L) | Single nucleotide variant (missense variant) | not specified | |
| | ARHGEF19, LOC129929521 (E325D) | Single nucleotide variant (missense variant) | not specified | |
| | ARHGEF19, LOC129929521 (S338I) | Single nucleotide variant (missense variant) | not specified | |
| | ARHGEF19, LOC129929521 (R342G) | Single nucleotide variant (missense variant) | not specified | |
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