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rs1057521793

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521793(A;A)
Make rs1057521793(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position111787102
GeneKCND3
is asnp
is mentioned by
dbSNPrs1057521793
dbSNP (classic)rs1057521793
ClinGenrs1057521793
ebirs1057521793
HLIrs1057521793
Exacrs1057521793
Gnomadrs1057521793
Varsomers1057521793
LitVarrs1057521793
Maprs1057521793
PheGenIrs1057521793
Biobankrs1057521793
1000 genomesrs1057521793
hgdprs1057521793
ensemblrs1057521793
geneviewrs1057521793
scholarrs1057521793
googlers1057521793
pharmgkbrs1057521793
gwascentralrs1057521793
openSNPrs1057521793
23andMers1057521793
23andMe allrs1057521793
SNPshotrs1057521793
SNPdbers1057521793
MSV3drs1057521793
GWAS Ctlgrs1057521793
Max Magnitude0
ClinVar
Risk rs1057521793(A;A)
Alt rs1057521793(A;A)
Reference Rs1057521793(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCND3
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.112329724C>T
CLNSRC
CLNACC RCV000430266.1,