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rs147914967

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs147914967(A;A)
Make rs147914967(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position46950389
GeneTTC7A
is asnp
is mentioned by
dbSNPrs147914967
ebirs147914967
HLIrs147914967
Exacrs147914967
Varsomers147914967
Maprs147914967
PheGenIrs147914967
hapmaprs147914967
1000 genomesrs147914967
hgdprs147914967
ensemblrs147914967
gopubmedrs147914967
geneviewrs147914967
scholarrs147914967
googlers147914967
pharmgkbrs147914967
gwascentralrs147914967
openSNPrs147914967
23andMers147914967
23andMe allrs147914967
SNP Nexus

SNPshotrs147914967
SNPdbers147914967
MSV3drs147914967
GWAS Ctlgrs147914967
Max Magnitude0
ClinVar
Risk rs147914967(A;A)
Alt rs147914967(A;A)
Reference rs147914967(G;G)
Significance Pathogenic
Disease Multiple gastrointestinal atresias
Variation info
Gene TTC7A
CLNDBN Multiple gastrointestinal atresias
Reversed 0
HGVS NC_000002.11:g.47177528G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000170533.2,