List of variants in gene ANOS1 reported as likely pathogenic for Kallmann syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000216.4(ANOS1):c.255+5G>A	rs773138384	0.00004
NC_000023.11:g.(?_8553932)_(8597276_?)dup
NM_000216.4(ANOS1):c.1063-1G>C	rs2146805381
NM_000216.4(ANOS1):c.1355-1G>T
NM_000216.4(ANOS1):c.1449+1G>A	rs1601946139
NM_000216.4(ANOS1):c.1449+1G>T
NM_000216.4(ANOS1):c.145T>C (p.Cys49Arg)	rs1057520209
NM_000216.4(ANOS1):c.171_174dup (p.Thr59fs)	rs1932981715
NM_000216.4(ANOS1):c.1904A>C (p.Gln635Pro)	rs1057519418
NM_000216.4(ANOS1):c.313del (p.Cys105fs)	rs1601988004
NM_000216.4(ANOS1):c.318+1G>C	rs2146846673
NM_000216.4(ANOS1):c.422G>A (p.Ser141Asn)	rs932845258
NM_000216.4(ANOS1):c.844del (p.Arg282fs)	rs2146817108

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