List of variants in gene DLX3 reported as benign for dental enamel hypoplasia

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_005220.3(DLX3):c.*928A>G	rs12452477	0.72043
NM_005220.3(DLX3):c.-64C>T	rs2278163	0.26785
NM_005220.3(DLX3):c.402G>A (p.Thr134=)	rs2303466	0.18221
NM_005220.3(DLX3):c.516+23C>T	rs2303467	0.18199
NM_005220.3(DLX3):c.*1326T>A	rs3803877	0.09111
NM_005220.3(DLX3):c.-134C>A	rs10459948	0.08249
NM_005220.3(DLX3):c.138C>T (p.Pro46=)	rs33937843	0.08182
NM_005220.3(DLX3):c.-189G>T	rs34783534	0.06775
NM_005220.3(DLX3):c.*1300C>G	rs3803878	0.06607
NM_005220.3(DLX3):c.*1016G>C	rs74607282	0.06204
NM_005220.3(DLX3):c.*494A>G	rs78617063	0.02070
NM_005220.3(DLX3):c.*679C>T	rs77798106	0.01827
NM_005220.3(DLX3):c.582G>A (p.Pro194=)	rs11868203	0.00824
NM_005220.3(DLX3):c.*986C>T	rs113406148	0.00384
NM_005220.3(DLX3):c.*527G>A	rs188986974	0.00290
NM_005220.3(DLX3):c.*1335C>T	rs529185809	0.00228
NM_005220.3(DLX3):c.*1410G>A	rs564135525	0.00206
NM_005220.3(DLX3):c.710A>G (p.Tyr237Cys)	rs142563930	0.00179
NM_005220.3(DLX3):c.*1296G>A	rs117813438	0.00066
NM_005220.3(DLX3):c.*707C>T	rs185357085	0.00056
NM_005220.3(DLX3):c.*868C>T	rs540375923	0.00043
NM_005220.3(DLX3):c.*60G>A	rs3744540	0.00029
NM_005220.3(DLX3):c.736G>C (p.Asp246His)	rs3744539	0.00023
NM_005220.3(DLX3):c.*723T>G	rs182361413	0.00016
NM_005220.3(DLX3):c.*259C>A	rs190141435	0.00009
NM_005220.3(DLX3):c.*987C>T	rs575910460

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