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rs774877657

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs774877657(C;T)
Make rs774877657(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position11222821
GeneDOCK6
is asnp
is mentioned by
dbSNPrs774877657
ebirs774877657
HLIrs774877657
Exacrs774877657
Varsomers774877657
Maprs774877657
PheGenIrs774877657
hapmaprs774877657
1000 genomesrs774877657
hgdprs774877657
ensemblrs774877657
gopubmedrs774877657
geneviewrs774877657
scholarrs774877657
googlers774877657
pharmgkbrs774877657
gwascentralrs774877657
openSNPrs774877657
23andMers774877657
23andMe allrs774877657
SNP Nexus

SNPshotrs774877657
SNPdbers774877657
MSV3drs774877657
GWAS Ctlgrs774877657
Max Magnitude0
ClinVar
Risk rs774877657(T;T)
Alt rs774877657(T;T)
Reference rs774877657(C;C)
Significance Pathogenic
Disease Adams-Oliver syndrome 2
Variation info
Gene DOCK6
CLNDBN Adams-Oliver syndrome 2
Reversed 0
HGVS NC_000019.9:g.11333497C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000239496.1,