List of variants in gene ARHGDIB studied for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001175.7(ARHGDIB):c.353A>G (p.Asp118Gly)	rs764957329	0.00002
NM_001175.7(ARHGDIB):c.404A>C (p.Lys135Thr)	rs1863969818	0.00002
NM_001175.7(ARHGDIB):c.445C>T (p.Arg149Trp)	rs1042106739	0.00001
NM_001175.7(ARHGDIB):c.271C>A (p.Leu91Met)	rs2497554828
NM_001175.7(ARHGDIB):c.376G>A (p.Val126Ile)
NM_001175.7(ARHGDIB):c.469A>G (p.Thr157Ala)
NM_001175.7(ARHGDIB):c.536C>G (p.Thr179Ser)

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