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rs876657392

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876657392(A;G)
Make rs876657392(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47006639
GeneTTC7A
is asnp
is mentioned by
dbSNPrs876657392
ebirs876657392
HLIrs876657392
Exacrs876657392
Varsomers876657392
Maprs876657392
PheGenIrs876657392
hapmaprs876657392
1000 genomesrs876657392
hgdprs876657392
ensemblrs876657392
gopubmedrs876657392
geneviewrs876657392
scholarrs876657392
googlers876657392
pharmgkbrs876657392
gwascentralrs876657392
openSNPrs876657392
23andMers876657392
23andMe allrs876657392
SNP Nexus

SNPshotrs876657392
SNPdbers876657392
MSV3drs876657392
GWAS Ctlgrs876657392
Max Magnitude0
ClinVar
Risk rs876657392(G;G)
Alt rs876657392(G;G)
Reference rs876657392(A;A)
Significance Pathogenic
Disease Multiple gastrointestinal atresias
Variation info
Gene TTC7A
CLNDBN Multiple gastrointestinal atresias
Reversed 0
HGVS NC_000002.11:g.47233778A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000170530.2,