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rs1057521154

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521154(G;T)
Make rs1057521154(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position16047905
GeneCLCNKB
is asnp
is mentioned by
dbSNPrs1057521154
dbSNP (old)rs1057521154
ClinGenrs1057521154
ebirs1057521154
HLIrs1057521154
Exacrs1057521154
Gnomadrs1057521154
Varsomers1057521154
LitVarrs1057521154
Maprs1057521154
PheGenIrs1057521154
Biobankrs1057521154
1000 genomesrs1057521154
hgdprs1057521154
ensemblrs1057521154
gopubmedrs1057521154
geneviewrs1057521154
scholarrs1057521154
googlers1057521154
pharmgkbrs1057521154
gwascentralrs1057521154
openSNPrs1057521154
23andMers1057521154
23andMe allrs1057521154
SNPshotrs1057521154
SNPdbers1057521154
MSV3drs1057521154
GWAS Ctlgrs1057521154
Max Magnitude0
ClinVar
Risk rs1057521154(T;T)
Alt rs1057521154(T;T)
Reference Rs1057521154(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CLCNKB
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.16374400G>T
CLNSRC
CLNACC RCV000438277.1,