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rs139010200

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs139010200(A;G)
Make rs139010200(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47046329
GeneTTC7A
is asnp
is mentioned by
dbSNPrs139010200
ebirs139010200
HLIrs139010200
Exacrs139010200
Varsomers139010200
Maprs139010200
PheGenIrs139010200
hapmaprs139010200
1000 genomesrs139010200
hgdprs139010200
ensemblrs139010200
gopubmedrs139010200
geneviewrs139010200
scholarrs139010200
googlers139010200
pharmgkbrs139010200
gwascentralrs139010200
openSNPrs139010200
23andMers139010200
23andMe allrs139010200
SNP Nexus

SNPshotrs139010200
SNPdbers139010200
MSV3drs139010200
GWAS Ctlgrs139010200
Max Magnitude0
ClinVar
Risk rs139010200(G;G)
Alt rs139010200(G;G)
Reference rs139010200(A;A)
Significance Pathogenic
Disease Multiple gastrointestinal atresias
Variation info
Gene TTC7A
CLNDBN Multiple gastrointestinal atresias
Reversed 0
HGVS NC_000002.11:g.47273468A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000170526.2,