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rs1085307773

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome18
Position53207745
GeneDCC
is asnp
is mentioned by
dbSNPrs1085307773
dbSNP (old)rs1085307773
ClinGenrs1085307773
ebirs1085307773
HLIrs1085307773
Exacrs1085307773
Gnomadrs1085307773
Varsomers1085307773
Maprs1085307773
PheGenIrs1085307773
Biobankrs1085307773
1000 genomesrs1085307773
hgdprs1085307773
ensemblrs1085307773
gopubmedrs1085307773
geneviewrs1085307773
scholarrs1085307773
googlers1085307773
pharmgkbrs1085307773
gwascentralrs1085307773
openSNPrs1085307773
23andMers1085307773
23andMe allrs1085307773
SNPshotrs1085307773
SNPdbers1085307773
MSV3drs1085307773
GWAS Ctlgrs1085307773
Max Magnitude0
ClinVar
Risk rs1085307773(T;T)
Alt rs1085307773(T;T)
Reference Rs1085307773(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DCC
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.50734115C>T
CLNSRC
CLNACC RCV000489691.1,