List of variants in gene LINGO1 studied for autosomal recessive disease

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_032808.7(LINGO1):c.714G>C (p.Leu238=)	rs2271396	0.65067
NM_032808.7(LINGO1):c.474A>G (p.Leu158=)	rs2271397	0.64965
NM_032808.7(LINGO1):c.465C>T (p.Ile155=)	rs2271398	0.64821
NM_032808.7(LINGO1):c.1104C>T (p.Ser368=)	rs3743481	0.43645
NM_032808.7(LINGO1):c.295G>A (p.Glu99Lys)	rs150289554	0.00040
NM_032808.7(LINGO1):c.70C>G (p.Gln24Glu)	rs772748227	0.00008
NM_032808.7(LINGO1):c.869G>A (p.Arg290His)	rs757077698	0.00003
NM_032808.7(LINGO1):c.1825G>A (p.Ala609Thr)	rs367728067	0.00001
NM_032808.7(LINGO1):c.863A>G (p.Tyr288Cys)	rs750612085	0.00001
NM_032808.7(LINGO1):c.868C>T (p.Arg290Cys)	rs767873726	0.00001
NM_032808.7(LINGO1):c.1406A>G (p.Lys469Arg)	rs868551107
NM_032808.7(LINGO1):c.158G>A (p.Arg53His)

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