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rs587777548

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777548(C;G)
Make rs587777548(G;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position46995142
GeneTTC7A
is asnp
is mentioned by
dbSNPrs587777548
ebirs587777548
HLIrs587777548
Exacrs587777548
Varsomers587777548
Maprs587777548
PheGenIrs587777548
hapmaprs587777548
1000 genomesrs587777548
hgdprs587777548
ensemblrs587777548
gopubmedrs587777548
geneviewrs587777548
scholarrs587777548
googlers587777548
pharmgkbrs587777548
gwascentralrs587777548
openSNPrs587777548
23andMers587777548
23andMe allrs587777548
SNP Nexus

SNPshotrs587777548
SNPdbers587777548
MSV3drs587777548
GWAS Ctlgrs587777548
Max Magnitude0
ClinVar
Risk rs587777548(G,T;G,T)
Alt rs587777548(G,T;G,T)
Reference rs587777548(C;C)
Significance Pathogenic
Disease Multiple gastrointestinal atresias
Variation info
Gene TTC7A
CLNDBN Multiple gastrointestinal atresias
Reversed 0
HGVS NC_000002.11:g.47222281C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000128795.3,