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rs587777549

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777549(-;-)
Make rs587777549(-;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position47021950
GeneTTC7A
is asnp
is mentioned by
dbSNPrs587777549
ebirs587777549
HLIrs587777549
Exacrs587777549
Varsomers587777549
Maprs587777549
PheGenIrs587777549
hapmaprs587777549
1000 genomesrs587777549
hgdprs587777549
ensemblrs587777549
gopubmedrs587777549
geneviewrs587777549
scholarrs587777549
googlers587777549
pharmgkbrs587777549
gwascentralrs587777549
openSNPrs587777549
23andMers587777549
23andMe allrs587777549
SNP Nexus

SNPshotrs587777549
SNPdbers587777549
MSV3drs587777549
GWAS Ctlgrs587777549
Max Magnitude0
ClinVar
Risk rs587777549(;)
Alt rs587777549(;)
Reference rs587777549(G;G)
Significance Pathogenic
Disease Multiple gastrointestinal atresias
Variation info
Gene TTC7A
CLNDBN Multiple gastrointestinal atresias
Reversed 0
HGVS NC_000002.11:g.47249089delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000128796.3,