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rs1057519056

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519056(C;C)
Make rs1057519056(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position53207746
GeneDCC
is asnp
is mentioned by
dbSNPrs1057519056
dbSNP (classic)rs1057519056
ClinGenrs1057519056
ebirs1057519056
HLIrs1057519056
Exacrs1057519056
Gnomadrs1057519056
Varsomers1057519056
LitVarrs1057519056
Maprs1057519056
PheGenIrs1057519056
Biobankrs1057519056
1000 genomesrs1057519056
hgdprs1057519056
ensemblrs1057519056
geneviewrs1057519056
scholarrs1057519056
googlers1057519056
pharmgkbrs1057519056
gwascentralrs1057519056
openSNPrs1057519056
23andMers1057519056
23andMe allrs1057519056
SNPshotrs1057519056
SNPdbers1057519056
MSV3drs1057519056
GWAS Ctlgrs1057519056
Max Magnitude0
ClinVar
Risk rs1057519056(C;C)
Alt rs1057519056(C;C)
Reference Rs1057519056(G;G)
Significance Pathogenic
Disease Corpus callosum agenesis
Variation info
Gene DCC
CLNDBN Corpus callosum agenesis
Reversed 0
HGVS NC_000018.9:g.50734116G>C
CLNSRC
CLNACC RCV000416340.1,