List of variants in gene GJB2 reported as benign

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: 41

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HGVS	dbSNP
NM_004004.5(GJB2):c.*1447G>A	rs11839674
NM_004004.5(GJB2):c.-216T>G	rs574815423
NM_004004.6(GJB2):c.*1016A>G	rs537683957
NM_004004.6(GJB2):c.*1033G>A	rs185790172
NM_004004.6(GJB2):c.*104A>T	rs7337074
NM_004004.6(GJB2):c.*1067G>T	rs9237
NM_004004.6(GJB2):c.*111C>T	rs7329857
NM_004004.6(GJB2):c.*1152G>A	rs7623
NM_004004.6(GJB2):c.*1197T>A	rs11841182
NM_004004.6(GJB2):c.*1277T>C	rs7988691
NM_004004.6(GJB2):c.*168A>G	rs55704559
NM_004004.6(GJB2):c.*1C>T	rs111033327
NM_004004.6(GJB2):c.*3C>A	rs111033460
NM_004004.6(GJB2):c.*786G>A	rs187158699
NM_004004.6(GJB2):c.*84T>C	rs3751385
NM_004004.6(GJB2):c.*931C>T	rs5030700
NM_004004.6(GJB2):c.-15C>T	rs72561725
NM_004004.6(GJB2):c.-22-12C>T	rs9578260
NM_004004.6(GJB2):c.-22-2A>C	rs201895089
NM_004004.6(GJB2):c.-22-6T>C	rs141962118
NM_004004.6(GJB2):c.-23+12G>A	rs397516866
NM_004004.6(GJB2):c.-45C>A	rs397516868
NM_004004.6(GJB2):c.-6T>A	rs148136545
NM_004004.6(GJB2):c.101T>C (p.Met34Thr)	rs35887622
NM_004004.6(GJB2):c.109G>A (p.Val37Ile)	rs72474224
NM_004004.6(GJB2):c.11G>A (p.Gly4Asp)	rs111033222
NM_004004.6(GJB2):c.249C>G (p.Phe83Leu)	rs111033218
NM_004004.6(GJB2):c.269T>C (p.Leu90Pro)	rs80338945
NM_004004.6(GJB2):c.341A>G (p.Glu114Gly)	rs2274083
NM_004004.6(GJB2):c.368C>A (p.Thr123Asn)	rs111033188
NM_004004.6(GJB2):c.380G>A (p.Arg127His)	rs111033196
NM_004004.6(GJB2):c.412A>G (p.Ser138Gly)	rs397516876
NM_004004.6(GJB2):c.416G>A (p.Ser139Asn)	rs76434661
NM_004004.6(GJB2):c.457G>A (p.Val153Ile)	rs111033186
NM_004004.6(GJB2):c.478G>A (p.Gly160Ser)	rs34988750
NM_004004.6(GJB2):c.493C>T (p.Arg165Trp)	rs376898963
NM_004004.6(GJB2):c.499G>A (p.Val167Met)	rs111033360
NM_004004.6(GJB2):c.510C>T (p.Asn170=)	rs763068053
NM_004004.6(GJB2):c.511G>A (p.Ala171Thr)	rs201004645
NM_004004.6(GJB2):c.608T>C (p.Ile203Thr)	rs76838169
NM_004004.6(GJB2):c.79G>A (p.Val27Ile)	rs2274084

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