ClinVar Miner

List of variants in gene HCN1 reported as benign for central nervous system disorder

Included ClinVar conditions (2490):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_021072.4(HCN1):c.1783+7dup rs56154381 0.04936
NM_021072.4(HCN1):c.1012-14A>G rs112775315 0.00521
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.1710C>T (p.Asn570=) rs141455774 0.00038
NM_021072.4(HCN1):c.124C>T (p.Pro42Ser) rs56164833 0.00035
NM_021072.4(HCN1):c.2227C>G (p.Pro743Ala) rs560701504 0.00032
NM_021072.4(HCN1):c.1626C>T (p.Cys542=) rs150863293 0.00023
NM_021072.4(HCN1):c.259C>T (p.Pro87Ser) rs370113959 0.00021
NM_021072.4(HCN1):c.159C>G (p.His53Gln) rs10066808 0.00019
NM_021072.4(HCN1):c.1041C>T (p.Tyr347=) rs140235085 0.00011
NM_021072.4(HCN1):c.1437G>A (p.Ala479=) rs372374391 0.00011
NM_021072.4(HCN1):c.2390T>G (p.Val797Gly) rs150936707 0.00010
NM_021072.4(HCN1):c.68C>T (p.Ala23Val) rs1060500096 0.00005
NM_021072.4(HCN1):c.84G>A (p.Thr28=) rs1377682866 0.00004
NM_021072.4(HCN1):c.261C>G (p.Pro87=) rs199612501 0.00003
NM_021072.4(HCN1):c.2231C>T (p.Pro744Leu) rs1252725512 0.00001
NM_021072.4(HCN1):c.828A>G (p.Arg276=) rs1417499521 0.00001
NM_021072.4(HCN1):c.1231-13C>T
NM_021072.4(HCN1):c.159C>A (p.His53Gln)
NM_021072.4(HCN1):c.192TGGCGGCGG[1] (p.Gly72_Gly74del) rs56064803
NM_021072.4(HCN1):c.203GCG[5] (p.Gly73_Gly74del) rs747975797
NM_021072.4(HCN1):c.252C>T (p.Ala84=) rs573050222
NM_021072.4(HCN1):c.2635C>A (p.Pro879Thr) rs761866949
NM_021072.4(HCN1):c.426-12del rs750563670
NM_021072.4(HCN1):c.426-12dup
NM_021072.4(HCN1):c.426-8_426-5del rs1394225411
NM_021072.4(HCN1):c.45C>T (p.Asp15=)

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