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rs863223404

From SNPedia

Orientationminus
Make rs863223404(A;GG)
Make rs863223404(GG;GG)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position55261478
GeneTCF4
is asnp
is mentioned by
dbSNPrs863223404
ebirs863223404
HLIrs863223404
Exacrs863223404
Varsomers863223404
Maprs863223404
PheGenIrs863223404
hapmaprs863223404
1000 genomesrs863223404
hgdprs863223404
ensemblrs863223404
gopubmedrs863223404
geneviewrs863223404
scholarrs863223404
googlers863223404
pharmgkbrs863223404
gwascentralrs863223404
openSNPrs863223404
23andMers863223404
23andMe allrs863223404
SNP Nexus

SNPshotrs863223404
SNPdbers863223404
MSV3drs863223404
GWAS Ctlgrs863223404
Max Magnitude
ClinVar
Risk rs863223404(GG;GG)
Alt rs863223404(GG;GG)
Reference rs863223404(A;A)
Significance Pathogenic
Disease Pitt-Hopkins syndrome
Variation info
Gene TCF4
CLNDBN Pitt-Hopkins syndrome
Reversed 1
HGVS NC_000018.9:g.52928709delTinsCC
CLNSRC
CLNACC RCV000194458.2,