List of variants in gene ANKRD26 reported as benign for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_014915.3(ANKRD26):c.2376-16A>G	rs7096505	0.83236
NM_014915.3(ANKRD26):c.624A>G (p.Val208=)	rs2297145	0.22780
NM_014915.3(ANKRD26):c.3913G>A (p.Val1305Ile)	rs10829163	0.19017
NM_014915.3(ANKRD26):c.4542T>A (p.Phe1514Leu)	rs2274741	0.19016
NM_014915.3(ANKRD26):c.3972+3A>G	rs72807627	0.08792
NM_014915.3(ANKRD26):c.-59G>A	rs3737056	0.07344
NM_014915.3(ANKRD26):c.-140C>G	rs41299222	0.05835
NM_014915.3(ANKRD26):c.1273A>G (p.Ile425Val)	rs12359281	0.04174
NM_014915.3(ANKRD26):c.1207+15A>G	rs115864032	0.03406
NM_014915.3(ANKRD26):c.2978A>C (p.Glu993Ala)	rs61745662	0.02396
NM_014915.3(ANKRD26):c.2376-4G>A	rs75445709	0.02272
NM_014915.3(ANKRD26):c.1564+6T>C	rs149655759	0.01710
NM_014915.3(ANKRD26):c.3384G>A (p.Lys1128=)	rs41299210	0.01449
NM_014915.3(ANKRD26):c.576G>A (p.Gln192=)	rs41279942	0.01351
NM_014915.3(ANKRD26):c.3658G>C (p.Val1220Leu)	rs12572862	0.01072
NM_014915.3(ANKRD26):c.3655G>A (p.Val1219Ile)	rs146819984	0.00781
NM_014915.2(ANKRD26):c.-184G>T	rs527666933	0.00525
NM_014915.3(ANKRD26):c.1747C>G (p.Gln583Glu)	rs56151272	0.00260
NM_014915.3(ANKRD26):c.2584C>G (p.Gln862Glu)	rs74128547	0.00260
NM_014915.3(ANKRD26):c.531+10A>T	rs114367485	0.00227
NM_014915.3(ANKRD26):c.2679A>G (p.Gln893=)	rs61730098	0.00215
NM_014915.3(ANKRD26):c.1133A>G (p.Glu378Gly)	rs186243874	0.00188
NM_014915.3(ANKRD26):c.3007G>A (p.Glu1003Lys)	rs41304587	0.00141
NM_014915.3(ANKRD26):c.4259G>A (p.Cys1420Tyr)	rs146159734	0.00138
NM_014915.3(ANKRD26):c.4145T>A (p.Phe1382Tyr)	rs78251061	0.00122
NM_014915.3(ANKRD26):c.4490T>A (p.Val1497Asp)	rs149647444	0.00037
NM_014915.3(ANKRD26):c.531+9C>G	rs142574680	0.00026
NM_014915.3(ANKRD26):c.-77C>G	rs546768605
NM_014915.3(ANKRD26):c.1462+17C>A	rs11015496
NM_014915.3(ANKRD26):c.1571A>G (p.His524Arg)	rs199656285
NM_014915.3(ANKRD26):c.1590AGA[2] (p.Glu533del)	rs138423863
NM_014915.3(ANKRD26):c.1986-3dup	rs113123391
NM_014915.3(ANKRD26):c.937G>T (p.Asp313Tyr)	rs61730102

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