List of variants in gene LRP5 reported by Laboratory of Gastroenterology and Hepatology, Radboud University Medical Center

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: 21

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HGVS	dbSNP	gnomAD frequency
NM_002335.4(LRP5):c.3107G>A (p.Arg1036Gln)	rs61889560	0.00207
NM_002335.4(LRP5):c.3403C>T (p.Arg1135Cys)	rs143396225	0.00032
NM_002335.4(LRP5):c.2724C>G (p.His908Gln)	rs143539498	0.00011
NM_002335.4(LRP5):c.4580C>T (p.Pro1527Leu)	rs80291963	0.00009
NM_002335.4(LRP5):c.4096G>A (p.Asp1366Asn)	rs779534615	0.00006
NM_002335.4(LRP5):c.1680G>T (p.Trp560Cys)	rs377144001	0.00004
NM_002335.4(LRP5):c.4268C>T (p.Pro1423Leu)	rs748143518	0.00003
NM_002335.4(LRP5):c.4225C>T (p.Arg1409Cys)	rs759834541	0.00002
NM_002335.4(LRP5):c.1948A>G (p.Thr650Ala)	rs756999448	0.00001
NM_002335.4(LRP5):c.2648A>G (p.Gln883Arg)	rs2098660959	0.00001
NM_002335.4(LRP5):c.4402G>A (p.Gly1468Ser)	rs764802790	0.00001
NM_002335.4(LRP5):c.441G>C (p.Trp147Cys)	rs748347747	0.00001
NM_002335.4(LRP5):c.4651G>A (p.Asp1551Asn)	rs724159827	0.00001
NM_002335.4(LRP5):c.1136A>C (p.Asp379Ala)	rs2153153124
NM_002335.4(LRP5):c.1360G>A (p.Val454Met)	rs373910016
NM_002335.4(LRP5):c.3468G>C (p.Gln1156His)	rs724159825
NM_002335.4(LRP5):c.34CTG[6] (p.Leu18_Leu20del)	rs72555376
NM_002335.4(LRP5):c.3562C>T (p.Arg1188Trp)	rs141178995
NM_002335.4(LRP5):c.3916G>T (p.Ala1306Ser)	rs748395267
NM_002335.4(LRP5):c.441G>T (p.Trp147Cys)	rs748347747
NM_002335.4(LRP5):c.4587G>C (p.Arg1529Ser)	rs724159826

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