List of variants in gene MSX2 reported as benign for Parietal foramina 1

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_002449.5(MSX2):c.*1176G>C	rs2890849	0.79238
NM_002449.5(MSX2):c.386T>C (p.Met129Thr)	rs4242182	0.78320
NM_002449.5(MSX2):c.*1125A>G	rs14459	0.76842
NM_002449.5(MSX2):c.*510A>G	rs2381939	0.76399
NM_002449.5(MSX2):c.*1146T>C	rs2890848	0.75720
NM_002449.5(MSX2):c.380-164G>A	rs4867776	0.56979
NM_002449.5(MSX2):c.*658C>T	rs10044147	0.03348
NM_002449.5(MSX2):c.-17C>G	rs4647952	0.03140
NM_002449.5(MSX2):c.*416A>C	rs10038500	0.02689
NM_002449.5(MSX2):c.*349T>C	rs114567531	0.02667
NM_002449.5(MSX2):c.*466G>A	rs148083483	0.00532
NM_002449.5(MSX2):c.*1007T>A	rs74292295	0.00387
NM_002449.5(MSX2):c.*257T>C	rs187794452	0.00376
NM_002449.5(MSX2):c.*723A>C	rs115604243	0.00315
NM_002449.5(MSX2):c.*1249T>C	rs139249455	0.00219
NM_002449.5(MSX2):c.*172G>A	rs577291689	0.00150
NM_002449.5(MSX2):c.*1050T>C	rs184931219	0.00119
NM_002449.5(MSX2):c.*635G>A	rs192627117	0.00093
NM_002449.5(MSX2):c.*157A>T	rs17063878	0.00045
NM_002449.5(MSX2):c.*878C>T	rs554272174	0.00034
NM_002449.5(MSX2):c.*1178C>T	rs182072112	0.00021
NM_002449.5(MSX2):c.699G>A (p.Ala233=)	rs201880865	0.00008
NM_002449.5(MSX2):c.-56C>A	rs113874536

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