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rs587777551

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777551(A;A)
Make rs587777551(A;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position47022084
GeneTTC7A
is asnp
is mentioned by
dbSNPrs587777551
ebirs587777551
HLIrs587777551
Exacrs587777551
Varsomers587777551
Maprs587777551
PheGenIrs587777551
hapmaprs587777551
1000 genomesrs587777551
hgdprs587777551
ensemblrs587777551
gopubmedrs587777551
geneviewrs587777551
scholarrs587777551
googlers587777551
pharmgkbrs587777551
gwascentralrs587777551
openSNPrs587777551
23andMers587777551
23andMe allrs587777551
SNP Nexus

SNPshotrs587777551
SNPdbers587777551
MSV3drs587777551
GWAS Ctlgrs587777551
Max Magnitude0
ClinVar
Risk rs587777551(A;A)
Alt rs587777551(A;A)
Reference rs587777551(T;T)
Significance Pathogenic
Disease Multiple gastrointestinal atresias
Variation info
Gene TTC7A
CLNDBN Multiple gastrointestinal atresias
Reversed 0
HGVS NC_000002.11:g.47249223T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000128798.3,