ClinVar Miner

List of variants reported as benign for MOGS-congenital disorder of glycosylation

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 17
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HGVS dbSNP gnomAD frequency
NM_006302.3(MOGS):c.877C>T (p.Pro293Ser) rs2268416 0.35953
NM_006302.3(MOGS):c.715G>A (p.Asp239Asn) rs1063588 0.33895
NM_006302.3(MOGS):c.184G>A (p.Val62Met) rs79181168 0.04027
NM_006302.3(MOGS):c.2032C>T (p.Arg678Trp) rs13405869 0.02517
NM_006302.3(MOGS):c.2353G>A (p.Gly785Ser) rs35533773 0.01925
NM_006302.3(MOGS):c.2017G>A (p.Val673Ile) rs114933392 0.01265
NM_006302.3(MOGS):c.1245C>G (p.Ile415Met) rs34838944 0.01053
NM_006302.3(MOGS):c.1838G>A (p.Arg613Gln) rs142032474 0.00643
NM_006302.3(MOGS):c.894C>T (p.Leu298=) rs146748462 0.00321
NM_006302.3(MOGS):c.881C>T (p.Pro294Leu) rs184209905 0.00318
NM_006302.3(MOGS):c.1944G>A (p.Glu648=) rs201547060 0.00113
NM_006302.3(MOGS):c.12C>G (p.Gly4=) rs555329045 0.00093
NM_006302.3(MOGS):c.85C>G (p.Arg29Gly) rs369653963 0.00044
NM_006302.3(MOGS):c.1587C>T (p.Asp529=) rs190772368 0.00016
NM_006302.3(MOGS):c.2112C>T (p.Pro704=) rs561758565 0.00003
NM_006302.3(MOGS):c.1158C>A (p.Gly386=) rs372087810
NM_006302.3(MOGS):c.876C>A (p.Ala292=) rs531051730

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