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rs1057521989

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521989(A;T)
Make rs1057521989(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position45461944
GeneHCN1
is asnp
is mentioned by
dbSNPrs1057521989
dbSNP (old)rs1057521989
ClinGenrs1057521989
ebirs1057521989
HLIrs1057521989
Exacrs1057521989
Gnomadrs1057521989
Varsomers1057521989
Maprs1057521989
PheGenIrs1057521989
Biobankrs1057521989
1000 genomesrs1057521989
hgdprs1057521989
ensemblrs1057521989
gopubmedrs1057521989
geneviewrs1057521989
scholarrs1057521989
googlers1057521989
pharmgkbrs1057521989
gwascentralrs1057521989
openSNPrs1057521989
23andMers1057521989
23andMe allrs1057521989
SNPshotrs1057521989
SNPdbers1057521989
MSV3drs1057521989
GWAS Ctlgrs1057521989
Max Magnitude0
ClinVar
Risk rs1057521989(T;T)
Alt rs1057521989(T;T)
Reference Rs1057521989(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HCN1
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.45462046T>A
CLNSRC
CLNACC RCV000444585.1,