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rs397509399

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509399(C;C)
Make rs397509399(C;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position11214650
GeneDOCK6
is asnp
is mentioned by
dbSNPrs397509399
ebirs397509399
HLIrs397509399
Exacrs397509399
Varsomers397509399
Maprs397509399
PheGenIrs397509399
hapmaprs397509399
1000 genomesrs397509399
hgdprs397509399
ensemblrs397509399
gopubmedrs397509399
geneviewrs397509399
scholarrs397509399
googlers397509399
pharmgkbrs397509399
gwascentralrs397509399
openSNPrs397509399
23andMers397509399
23andMe allrs397509399
SNP Nexus

SNPshotrs397509399
SNPdbers397509399
MSV3drs397509399
GWAS Ctlgrs397509399
Max Magnitude0
ClinVar
Risk rs397509399(C;C)
Alt rs397509399(C;C)
Reference rs397509399(G;G)
Significance Pathogenic
Disease Adams-Oliver syndrome 2
Variation info
Gene DOCK6 LOC105372273
CLNDBN Adams-Oliver syndrome 2
Reversed 1
HGVS NC_000019.9:g.11325326C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000049240.2,