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rs777469885

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs777469885(G;T)
Make rs777469885(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position46994356
GeneTTC7A
is asnp
is mentioned by
dbSNPrs777469885
ebirs777469885
HLIrs777469885
Exacrs777469885
Varsomers777469885
Maprs777469885
PheGenIrs777469885
hapmaprs777469885
1000 genomesrs777469885
hgdprs777469885
ensemblrs777469885
gopubmedrs777469885
geneviewrs777469885
scholarrs777469885
googlers777469885
pharmgkbrs777469885
gwascentralrs777469885
openSNPrs777469885
23andMers777469885
23andMe allrs777469885
SNP Nexus

SNPshotrs777469885
SNPdbers777469885
MSV3drs777469885
GWAS Ctlgrs777469885
Max Magnitude0
ClinVar
Risk rs777469885(T;T)
Alt rs777469885(T;T)
Reference rs777469885(G;G)
Significance Pathogenic
Disease Multiple gastrointestinal atresias
Variation info
Gene TTC7A
CLNDBN Multiple gastrointestinal atresias
Reversed 0
HGVS NC_000002.11:g.47221495G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000170529.2,