List of variants in gene AGL reported as benign 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
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_000642.3(AGL):c.894C>T (p.Leu298=)	rs2230306	0.76251
NM_000642.3(AGL):c.959-18G>A	rs634880	0.73702
NM_000642.3(AGL):c.3259+37G>A	rs594249	0.65860
NM_000642.3(AGL):c.2812+11G>A	rs555929	0.65828
NM_000642.3(AGL):c.2001+8T>C	rs3736296	0.51012
NM_000642.3(AGL):c.2950-21T>A	rs2035961	0.48240
NM_000642.3(AGL):c.3836+45G>A	rs2274570	0.46505
NM_000642.3(AGL):c.-10A>G	rs2307130	0.41188
NM_000642.3(AGL):c.1424-44A>G	rs2291638	0.29229
NM_000642.3(AGL):c.83-33C>T	rs2307129	0.24077
NM_000642.3(AGL):c.3199C>T (p.Pro1067Ser)	rs3753494	0.13698
NM_000642.3(AGL):c.3343G>A (p.Gly1115Arg)	rs2230307	0.05399
NM_000642.3(AGL):c.3700+32T>C	rs834575	0.05338
NM_000642.3(AGL):c.686A>G (p.Gln229Arg)	rs17121403	0.04398
NM_000642.3(AGL):c.3588+36T>G	rs548255	0.01966
NM_000642.3(AGL):c.1185+15T>C	rs17121466	0.01894
NM_000642.3(AGL):c.1155G>T (p.Lys385Asn)	rs28730701	0.01764
NM_000642.3(AGL):c.207T>C (p.Asn69=)	rs2230305	0.01529
NM_000642.3(AGL):c.112A>G (p.Thr38Ala)	rs35278779	0.01527
NM_000642.3(AGL):c.2885C>G (p.Ser962Cys)	rs34714252	0.01465
NM_000642.3(AGL):c.1160G>A (p.Arg387Gln)	rs17121464	0.01447
NM_000642.3(AGL):c.3849T>C (p.Ala1283=)	rs28730706	0.01312
NM_000642.3(AGL):c.3260-19G>A	rs140333425	0.01279
NM_000642.3(AGL):c.3619G>A (p.Ala1207Thr)	rs11807956	0.00940
NM_000642.3(AGL):c.2802A>C (p.Ala934=)	rs34230588	0.00775
NM_000642.3(AGL):c.1481G>A (p.Arg494His)	rs141043166	0.00743
NM_000642.3(AGL):c.3758G>A (p.Arg1253His)	rs12043139	0.00515
NM_000642.3(AGL):c.3384G>A (p.Ala1128=)	rs149393587	0.00383
NM_000642.3(AGL):c.2883A>G (p.Arg961=)	rs113625417	0.00375
NM_000642.3(AGL):c.3260-20T>C	rs17121560	0.00332
NM_000642.3(AGL):c.2522C>T (p.Ser841Phe)	rs150441555	0.00209
NM_000642.3(AGL):c.3203A>G (p.Tyr1068Cys)	rs147165298	0.00193
NM_000642.3(AGL):c.4162-11G>A	rs184309460

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