Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057519054

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519054(G;G)
Make rs1057519054(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position53386061
GeneDCC
is asnp
is mentioned by
dbSNPrs1057519054
dbSNP (classic)rs1057519054
ClinGenrs1057519054
ebirs1057519054
HLIrs1057519054
Exacrs1057519054
Gnomadrs1057519054
Varsomers1057519054
LitVarrs1057519054
Maprs1057519054
PheGenIrs1057519054
Biobankrs1057519054
1000 genomesrs1057519054
hgdprs1057519054
ensemblrs1057519054
geneviewrs1057519054
scholarrs1057519054
googlers1057519054
pharmgkbrs1057519054
gwascentralrs1057519054
openSNPrs1057519054
23andMers1057519054
SNPshotrs1057519054
SNPdbers1057519054
MSV3drs1057519054
GWAS Ctlgrs1057519054
Max Magnitude0
ClinVar
Risk rs1057519054(G;G)
Alt rs1057519054(G;G)
Reference Rs1057519054(T;T)
Significance Pathogenic
Disease Corpus callosum agenesis
Variation info
Gene DCC
CLNDBN Corpus callosum agenesis
Reversed 0
HGVS NC_000018.9:g.50912431T>G
CLNSRC
CLNACC RCV000416336.1,