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rs397509398

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397509398(-;-)
Make rs397509398(-;T)
Make rs397509398(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position11235631
GeneDOCK6
is asnp
is mentioned by
dbSNPrs397509398
ebirs397509398
HLIrs397509398
Exacrs397509398
Varsomers397509398
Maprs397509398
PheGenIrs397509398
hapmaprs397509398
1000 genomesrs397509398
hgdprs397509398
ensemblrs397509398
gopubmedrs397509398
geneviewrs397509398
scholarrs397509398
googlers397509398
pharmgkbrs397509398
gwascentralrs397509398
openSNPrs397509398
23andMers397509398
23andMe allrs397509398
SNP Nexus

SNPshotrs397509398
SNPdbers397509398
MSV3drs397509398
GWAS Ctlgrs397509398
Max Magnitude0
ClinVar
Risk rs397509398(T;T)
Alt rs397509398(T;T)
Reference rs397509398(;)
Significance Pathogenic
Disease Adams-Oliver syndrome 2
Variation info
Gene DOCK6
CLNDBN Adams-Oliver syndrome 2
Reversed 1
HGVS NC_000019.9:g.11346308dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000049239.3,