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rs1057518007

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518007(C;C)
Make rs1057518007(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position111787018
GeneKCND3
is asnp
is mentioned by
dbSNPrs1057518007
dbSNP (old)rs1057518007
ClinGenrs1057518007
ebirs1057518007
HLIrs1057518007
Exacrs1057518007
Gnomadrs1057518007
Varsomers1057518007
LitVarrs1057518007
Maprs1057518007
PheGenIrs1057518007
Biobankrs1057518007
1000 genomesrs1057518007
hgdprs1057518007
ensemblrs1057518007
gopubmedrs1057518007
geneviewrs1057518007
scholarrs1057518007
googlers1057518007
pharmgkbrs1057518007
gwascentralrs1057518007
openSNPrs1057518007
23andMers1057518007
23andMe allrs1057518007
SNPshotrs1057518007
SNPdbers1057518007
MSV3drs1057518007
GWAS Ctlgrs1057518007
Max Magnitude0
ClinVar
Risk rs1057518007(C;C)
Alt rs1057518007(C;C)
Reference Rs1057518007(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCND3
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.112329640C>G
CLNSRC
CLNACC RCV000413161.1,