List of variants in gene combination ALDOA, LOC112694756 reported as likely benign for not specified

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_001365304.2(LOC112694756):c.*1134-20G>A	rs75559164	0.00071
NM_001243177.4(ALDOA):c.1182A>G (p.Gln394=)	rs143419532	0.00046
NM_001365304.2(LOC112694756):c.150+18G>C	rs914905804	0.00026
NM_001365304.2(LOC112694756):c.*1309-20G>A	rs189723657	0.00025
NM_001365304.2(LOC112694756):c.*1308+12A>G	rs200733968	0.00014
NM_001365304.2(LOC112694756):c.-25G>A	rs774449859	0.00006
NM_001243177.4(ALDOA):c.1002G>A (p.Ala334=)	rs532473202	0.00005
NM_001243177.4(ALDOA):c.585C>T (p.Asp195=)	rs150741747	0.00005
NM_001243177.4(ALDOA):c.591T>C (p.Ala197=)	rs751360534	0.00004
NM_001365304.2(LOC112694756):c.7-4C>G	rs554730607	0.00004
NM_001365304.2(LOC112694756):c.*1134-15C>G	rs920112127	0.00003
NM_001365304.2(LOC112694756):c.*834-9C>T	rs1057523259	0.00003
NM_001243177.4(ALDOA):c.192G>A (p.Pro64=)	rs760287676	0.00002
NM_001243177.4(ALDOA):c.498C>T (p.Gly166=)	rs145811469	0.00002
NM_001243177.4(ALDOA):c.597C>T (p.Phe199=)	rs769378422	0.00002
NM_001243177.4(ALDOA):c.1032C>T (p.Cys344=)	rs767840312	0.00001
NM_001243177.4(ALDOA):c.1134G>A (p.Ala378=)	rs530089317	0.00001
NM_001365304.2(LOC112694756):c.*407-5C>T	rs1013012373	0.00001
NM_001365304.2(LOC112694756):c.-2C>T	rs1393272651	0.00001
NM_001365304.2(LOC112694756):c.20C>T (p.Pro7Leu)	rs566612278	0.00001
NM_001243177.4(ALDOA):c.225C>T (p.His75=)	rs11553110
NM_001365304.2(LOC112694756):c.*1308+11C>T	rs1057523917
NM_001365304.2(LOC112694756):c.*1308+17T>C	rs566755208
NM_001365304.2(LOC112694756):c.*422T>G	rs1026737159
NM_001365304.2(LOC112694756):c.*488+15dup	rs964620994
NM_001365304.2(LOC112694756):c.-46C>T	rs1057521393

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