List of variants reported as pathogenic for loose anagen syndrome

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_007373.4(SHOC2):c.4A>G (p.Ser2Gly)	rs267607048	0.00001
NM_002709.3(PPP1CB):c.146C>G (p.Pro49Arg)	rs886037952
NM_002709.3(PPP1CB):c.166G>C (p.Ala56Pro)	rs1114167429
NM_002709.3(PPP1CB):c.548A>C (p.Glu183Ala)	rs886037954
NM_002709.3(PPP1CB):c.548A>T (p.Glu183Val)	rs886037954
NM_002709.3(PPP1CB):c.658C>T (p.Arg220Cys)	rs1553311527
NM_002709.3(PPP1CB):c.820G>A (p.Glu274Lys)	rs886037955
NM_007373.4(SHOC2):c.517A>G (p.Met173Val)	rs1057518206
NM_007373.4(SHOC2):c.519G>A (p.Met173Ile)	rs730881020
NM_007373.4(SHOC2):c.806A>G (p.Gln269Arg)	rs864309599
NM_007373.4(SHOC2):c.807_808delinsTT (p.Gln269_His270delinsHisTyr)	rs1848064627

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