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rs199651452

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199651452(A;T)
Make rs199651452(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position53339775
GeneDCC
is asnp
is mentioned by
dbSNPrs199651452
dbSNP (classic)rs199651452
ClinGenrs199651452
ebirs199651452
HLIrs199651452
Exacrs199651452
Gnomadrs199651452
Varsomers199651452
LitVarrs199651452
Maprs199651452
PheGenIrs199651452
Biobankrs199651452
1000 genomesrs199651452
hgdprs199651452
ensemblrs199651452
geneviewrs199651452
scholarrs199651452
googlers199651452
pharmgkbrs199651452
gwascentralrs199651452
openSNPrs199651452
23andMers199651452
SNPshotrs199651452
SNPdbers199651452
MSV3drs199651452
GWAS Ctlgrs199651452
Max Magnitude0
ClinVar
Risk rs199651452(T;T)
Alt rs199651452(T;T)
Reference Rs199651452(A;A)
Significance Pathogenic
Disease Corpus callosum agenesis
Variation info
Gene DCC
CLNDBN Corpus callosum agenesis
Reversed 0
HGVS NC_000018.9:g.50866145A>T
CLNSRC
CLNACC RCV000416358.1,