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

rs769068305

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs769068305(C;G)
Make rs769068305(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position209788614
GeneIRF6
is asnp
is mentioned by
dbSNPrs769068305
ebirs769068305
HLIrs769068305
Exacrs769068305
Varsomers769068305
Maprs769068305
PheGenIrs769068305
hapmaprs769068305
1000 genomesrs769068305
hgdprs769068305
ensemblrs769068305
gopubmedrs769068305
geneviewrs769068305
scholarrs769068305
googlers769068305
pharmgkbrs769068305
gwascentralrs769068305
openSNPrs769068305
23andMers769068305
23andMe allrs769068305
SNP Nexus

SNPshotrs769068305
SNPdbers769068305
MSV3drs769068305
GWAS Ctlgrs769068305
Max Magnitude0
ClinVar
Risk rs769068305(G;G)
Alt rs769068305(G;G)
Reference rs769068305(C;C)
Significance Pathogenic
Disease Van der Woude syndrome
Variation info
Gene IRF6
CLNDBN Van der Woude syndrome
Reversed 0
HGVS NC_000001.10:g.209961959C>T
CLNSRC
CLNACC RCV000201948.1,