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rs876657393

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657393(A;A)
Make rs876657393(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47073840
GeneTTC7A
is asnp
is mentioned by
dbSNPrs876657393
ebirs876657393
HLIrs876657393
Exacrs876657393
Varsomers876657393
Maprs876657393
PheGenIrs876657393
hapmaprs876657393
1000 genomesrs876657393
hgdprs876657393
ensemblrs876657393
gopubmedrs876657393
geneviewrs876657393
scholarrs876657393
googlers876657393
pharmgkbrs876657393
gwascentralrs876657393
openSNPrs876657393
23andMers876657393
23andMe allrs876657393
SNP Nexus

SNPshotrs876657393
SNPdbers876657393
MSV3drs876657393
GWAS Ctlgrs876657393
Max Magnitude0
ClinVar
Risk rs876657393(A;A)
Alt rs876657393(A;A)
Reference rs876657393(G;G)
Significance Pathogenic
Disease Multiple gastrointestinal atresias
Variation info
Gene TTC7A
CLNDBN Multiple gastrointestinal atresias
Reversed 0
HGVS NC_000002.11:g.47300979G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000170532.2,