List of variants in gene HCN1 reported as benign for not provided

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_021072.4(HCN1):c.426-128T>A	rs76055011	0.06963
NM_021072.4(HCN1):c.1783+7dup	rs56154381	0.04936
NM_021072.4(HCN1):c.1012-214A>G	rs75449215	0.03660
NM_021072.4(HCN1):c.1230+104A>G	rs75228534	0.03417
NM_021072.4(HCN1):c.1231-100_1231-99del	rs113202045	0.02479
NM_021072.4(HCN1):c.-55G>T	rs184241507	0.01849
NM_021072.4(HCN1):c.1618+29A>G	rs16902099	0.01768
NM_021072.4(HCN1):c.1797A>G (p.Ser599=)	rs148932124	0.00419
NM_021072.4(HCN1):c.140G>T (p.Gly47Val)	rs544994462	0.00362
NM_021072.4(HCN1):c.1783+4C>T	rs188586020	0.00196
NM_021072.4(HCN1):c.2172C>T (p.Ala724=)	rs56217199	0.00191
NM_021072.4(HCN1):c.1619-3T>C	rs376434225	0.00062
NM_021072.4(HCN1):c.240C>A (p.Gly80=)	rs373664268	0.00032
NM_021072.4(HCN1):c.159C>G (p.His53Gln)	rs10066808	0.00019
NM_021072.4(HCN1):c.1041C>T (p.Tyr347=)	rs140235085	0.00011
GRCh37/hg19 5p12(chr5:45477535-45527688)x0
GRCh37/hg19 5p12(chr5:45527038-45527579)x1
GRCh37/hg19 5p12(chr5:45527038-45537620)x1
GRCh37/hg19 5p12(chr5:45527094-45527688)x0
GRCh37/hg19 5p12(chr5:45527094-45527826)x1
GRCh37/hg19 5p12(chr5:45527160-45537620)x1
GRCh37/hg19 5p12-11(chr5:45378207-46228333)x3
NM_021072.4(HCN1):c.1230+94dup	rs35841808
NM_021072.4(HCN1):c.1231-245A>G	rs79491080
NM_021072.4(HCN1):c.1619-211_1619-210insTA	rs1554014669
NM_021072.4(HCN1):c.1619-224dup	rs375114789
NM_021072.4(HCN1):c.192TGGCGGCGG[1] (p.Gly72_Gly74del)	rs56064803
NM_021072.4(HCN1):c.203GCG[4] (p.Gly72_Gly74del)	rs747975797
NM_021072.4(HCN1):c.203GCG[5] (p.Gly73_Gly74del)	rs747975797
NM_021072.4(HCN1):c.203GCG[6] (p.Gly74del)	rs747975797

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