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rs775565634

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs775565634(A;A)
Make rs775565634(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position53339808
GeneDCC
is asnp
is mentioned by
dbSNPrs775565634
dbSNP (classic)rs775565634
ClinGenrs775565634
ebirs775565634
HLIrs775565634
Exacrs775565634
Gnomadrs775565634
Varsomers775565634
LitVarrs775565634
Maprs775565634
PheGenIrs775565634
Biobankrs775565634
1000 genomesrs775565634
hgdprs775565634
ensemblrs775565634
geneviewrs775565634
scholarrs775565634
googlers775565634
pharmgkbrs775565634
gwascentralrs775565634
openSNPrs775565634
23andMers775565634
SNPshotrs775565634
SNPdbers775565634
MSV3drs775565634
GWAS Ctlgrs775565634
Max Magnitude0
ClinVar
Risk rs775565634(A;A)
Alt rs775565634(A;A)
Reference Rs775565634(G;G)
Significance Pathogenic
Disease Corpus callosum agenesis
Variation info
Gene DCC
CLNDBN Corpus callosum agenesis
Reversed 0
HGVS NC_000018.9:g.50866178G>A
CLNSRC
CLNACC RCV000416318.1,