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

rs1057519058

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519058(A;G)
Make rs1057519058(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position53467923
GeneDCC
is asnp
is mentioned by
dbSNPrs1057519058
dbSNP (old)rs1057519058
ClinGenrs1057519058
ebirs1057519058
HLIrs1057519058
Exacrs1057519058
Gnomadrs1057519058
Varsomers1057519058
LitVarrs1057519058
Maprs1057519058
PheGenIrs1057519058
Biobankrs1057519058
1000 genomesrs1057519058
hgdprs1057519058
ensemblrs1057519058
gopubmedrs1057519058
geneviewrs1057519058
scholarrs1057519058
googlers1057519058
pharmgkbrs1057519058
gwascentralrs1057519058
openSNPrs1057519058
23andMers1057519058
23andMe allrs1057519058
SNPshotrs1057519058
SNPdbers1057519058
MSV3drs1057519058
GWAS Ctlgrs1057519058
Max Magnitude0
ClinVar
Risk rs1057519058(G;G)
Alt rs1057519058(G;G)
Reference Rs1057519058(A;A)
Significance Pathogenic
Disease Corpus callosum agenesis
Variation info
Gene DCC
CLNDBN Corpus callosum agenesis
Reversed 0
HGVS NC_000018.9:g.50994293A>G
CLNSRC
CLNACC RCV000416369.1,