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rs149602485

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs149602485(C;C)
Make rs149602485(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47050043
GeneTTC7A
is asnp
is mentioned by
dbSNPrs149602485
ebirs149602485
HLIrs149602485
Exacrs149602485
Varsomers149602485
Maprs149602485
PheGenIrs149602485
hapmaprs149602485
1000 genomesrs149602485
hgdprs149602485
ensemblrs149602485
gopubmedrs149602485
geneviewrs149602485
scholarrs149602485
googlers149602485
pharmgkbrs149602485
gwascentralrs149602485
openSNPrs149602485
23andMers149602485
23andMe allrs149602485
SNP Nexus

SNPshotrs149602485
SNPdbers149602485
MSV3drs149602485
GWAS Ctlgrs149602485
Max Magnitude0
ClinVar
Risk rs149602485(C;C)
Alt rs149602485(C;C)
Reference rs149602485(T;T)
Significance Pathogenic
Disease Multiple gastrointestinal atresias
Variation info
Gene TTC7A
CLNDBN Multiple gastrointestinal atresias
Reversed 0
HGVS NC_000002.11:g.47277182T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000170526.2,