List of variants in gene ARHGAP26 reported as not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001135608.3(ARHGAP26):c.1107T>C (p.Pro369=)	rs139391817	0.00019
NM_001135608.3(ARHGAP26):c.1829C>T (p.Thr610Ile)	rs200573018	0.00003
NM_001135608.3(ARHGAP26):c.2185G>A (p.Asp729Asn)	rs587778049	0.00001
NM_001135608.3(ARHGAP26):c.1245delinsGTGGGG (p.Val416fs)	rs587778047
NM_001135608.3(ARHGAP26):c.1775A>G (p.Lys592Arg)	rs587778048
NM_001135608.3(ARHGAP26):c.2099+69A>G	rs562055157
NM_001135608.3(ARHGAP26):c.307C>T (p.Arg103Trp)	rs587778050

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