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

rs1085307991

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome7
Position50544015
GeneDDC
is asnp
is mentioned by
dbSNPrs1085307991
dbSNP (old)rs1085307991
ClinGenrs1085307991
ebirs1085307991
HLIrs1085307991
Exacrs1085307991
Gnomadrs1085307991
Varsomers1085307991
Maprs1085307991
PheGenIrs1085307991
Biobankrs1085307991
1000 genomesrs1085307991
hgdprs1085307991
ensemblrs1085307991
gopubmedrs1085307991
geneviewrs1085307991
scholarrs1085307991
googlers1085307991
pharmgkbrs1085307991
gwascentralrs1085307991
openSNPrs1085307991
23andMers1085307991
23andMe allrs1085307991
SNPshotrs1085307991
SNPdbers1085307991
MSV3drs1085307991
GWAS Ctlgrs1085307991
Max Magnitude0
ClinVar
Risk rs1085307991(C;C)
Alt rs1085307991(C;C)
Reference Rs1085307991(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DDC
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.50611713A>G
CLNSRC
CLNACC RCV000489419.1,