List of variants in gene VANGL1 reported as benign for congenital nervous system disorder

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_138959.3(VANGL1):c.*505A>G	rs6700610	0.67885
NM_138959.3(VANGL1):c.*2351T>G	rs12121158	0.41872
NM_138959.3(VANGL1):c.*3496T>A	rs4839472	0.31126
NM_138959.3(VANGL1):c.*416G>A	rs3811011	0.25321
NM_138959.3(VANGL1):c.*1277C>T	rs3204955	0.25318
NM_138959.3(VANGL1):c.*3023G>T	rs10923204	0.24904
NM_138959.3(VANGL1):c.*83T>A	rs3811013	0.17099
NM_138959.3(VANGL1):c.346G>A (p.Ala116Thr)	rs4839469	0.12684
NM_138959.3(VANGL1):c.-224C>A	rs191609592	0.10807
NM_138959.3(VANGL1):c.*2581G>A	rs3811008	0.10587
NM_138959.3(VANGL1):c.*3417C>T	rs76160883	0.06248
NM_138959.3(VANGL1):c.*2489C>T	rs41299571	0.06245
NM_138959.3(VANGL1):c.*300C>T	rs41310108	0.05806
NM_138959.3(VANGL1):c.*217C>T	rs41299565	0.05793
NM_138959.3(VANGL1):c.*694C>A	rs41312690	0.05722
NM_138959.3(VANGL1):c.*2043C>T	rs74117021	0.02749
NM_138959.3(VANGL1):c.1040A>C (p.Glu347Ala)	rs34059106	0.01695
NM_138959.3(VANGL1):c.*1627A>G	rs149888685	0.00606
NM_138959.3(VANGL1):c.285C>T (p.Ile95=)	rs140451005	0.00060
NM_138959.3(VANGL1):c.248C>T (p.Ser83Leu)	rs146695372	0.00010
NM_138959.3(VANGL1):c.518G>A (p.Arg173His)	rs148341022	0.00003
NM_138959.3(VANGL1):c.*1749G>T	rs3811010
NM_138959.3(VANGL1):c.*313A>G	rs3811012
NM_138959.3(VANGL1):c.-226G>C	rs116216703

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