ClinVar Miner

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

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Gene type:
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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_018341.3(ERMARD):c.1617C>T (p.Ile539=) rs4716399 0.30166
NM_018341.3(ERMARD):c.1618A>G (p.Ser540Gly) rs4716346 0.30164
NM_018341.3(ERMARD):c.858-10A>C rs9478006 0.19730
NM_018341.3(ERMARD):c.6+7C>T rs3749882 0.17754
NM_018341.3(ERMARD):c.870C>T (p.Cys290=) rs11966349 0.14834
NM_018341.3(ERMARD):c.1505G>A (p.Arg502His) rs41265401 0.08157
NM_018341.3(ERMARD):c.1739+18T>C rs79997179 0.07456
NM_018341.3(ERMARD):c.1233+10A>G rs17860640 0.06562
NM_018341.3(ERMARD):c.1060-12A>G rs111551747 0.01905
NM_018341.3(ERMARD):c.1944A>G (p.Thr648=) rs2274952 0.01821
NM_018341.3(ERMARD):c.9A>C (p.Val3=) rs61736820 0.01485
NM_018341.3(ERMARD):c.1014T>C (p.Asp338=) rs61747671 0.01263
NM_018341.3(ERMARD):c.274A>G (p.Ile92Val) rs17860632 0.01166
NM_018341.3(ERMARD):c.257C>A (p.Thr86Asn) rs61735516 0.00917
NM_018341.3(ERMARD):c.858-11C>T rs111558820 0.00898
NM_018341.3(ERMARD):c.1112A>G (p.His371Arg) rs61738268 0.00801
NM_018341.3(ERMARD):c.819A>G (p.Pro273=) rs149907871 0.00464
NM_018341.3(ERMARD):c.5A>T (p.Glu2Val) rs200330797 0.00424
NM_018341.3(ERMARD):c.1162A>G (p.Asn388Asp) rs151283330 0.00282
NM_018341.3(ERMARD):c.1246G>A (p.Val416Ile) rs143351214 0.00145
NM_018341.3(ERMARD):c.1480C>G (p.Arg494Gly) rs144908519 0.00131
NM_018341.3(ERMARD):c.241C>T (p.His81Tyr) rs137971039 0.00081

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