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rs202058123

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs202058123(A;A)
Make rs202058123(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position15445606
GeneCTRC
is asnp
is mentioned by
dbSNPrs202058123
dbSNP (old)rs202058123
ClinGenrs202058123
ebirs202058123
HLIrs202058123
Exacrs202058123
Gnomadrs202058123
Varsomers202058123
Maprs202058123
PheGenIrs202058123
Biobankrs202058123
1000 genomesrs202058123
hgdprs202058123
ensemblrs202058123
gopubmedrs202058123
geneviewrs202058123
scholarrs202058123
googlers202058123
pharmgkbrs202058123
gwascentralrs202058123
openSNPrs202058123
23andMers202058123
23andMe allrs202058123
SNPshotrs202058123
SNPdbers202058123
MSV3drs202058123
GWAS Ctlgrs202058123
Max Magnitude0
ClinVar
Risk rs202058123(A;A) rs202058123(C;C)
Alt rs202058123(A;A) rs202058123(C;C)
Reference Rs202058123(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene CTRC
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.15772101G>A; NC_000001.10:g.15772101G>C
CLNSRC
CLNACC RCV000493312.1, RCV000483666.1,