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rs786205698

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205698(C;T)
Make rs786205698(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47024294
GeneTTC7A
is asnp
is mentioned by
dbSNPrs786205698
ebirs786205698
HLIrs786205698
Exacrs786205698
Varsomers786205698
Maprs786205698
PheGenIrs786205698
hapmaprs786205698
1000 genomesrs786205698
hgdprs786205698
ensemblrs786205698
gopubmedrs786205698
geneviewrs786205698
scholarrs786205698
googlers786205698
pharmgkbrs786205698
gwascentralrs786205698
openSNPrs786205698
23andMers786205698
23andMe allrs786205698
SNP Nexus

SNPshotrs786205698
SNPdbers786205698
MSV3drs786205698
GWAS Ctlgrs786205698
Max Magnitude0
ClinVar
Risk rs786205698(T;T)
Alt rs786205698(T;T)
Reference rs786205698(C;C)
Significance Pathogenic
Disease Multiple gastrointestinal atresias
Variation info
Gene TTC7A
CLNDBN Multiple gastrointestinal atresias
Reversed 0
HGVS NC_000002.11:g.47251433C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000170531.2,