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rs587776971

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGT;AAGT) 0 common in clinvar
Make rs587776971(-;-)
Make rs587776971(-;AAGT)
ReferenceGRCh38 38.1/142
Chromosome2
Position46994513
GeneTTC7A
is asnp
is mentioned by
dbSNPrs587776971
ebirs587776971
HLIrs587776971
Exacrs587776971
Varsomers587776971
Maprs587776971
PheGenIrs587776971
hapmaprs587776971
1000 genomesrs587776971
hgdprs587776971
ensemblrs587776971
gopubmedrs587776971
geneviewrs587776971
scholarrs587776971
googlers587776971
pharmgkbrs587776971
gwascentralrs587776971
openSNPrs587776971
23andMers587776971
23andMe allrs587776971
SNP Nexus

SNPshotrs587776971
SNPdbers587776971
MSV3drs587776971
GWAS Ctlgrs587776971
Max Magnitude0
ClinVar
Risk rs587776971(;)
Alt rs587776971(;)
Reference rs587776971(AAGT;AAGT)
Significance Pathogenic
Disease Multiple gastrointestinal atresias
Variation info
Gene TTC7A
CLNDBN Multiple gastrointestinal atresias
Reversed 0
HGVS NC_000002.11:g.47221652_47221655delAAGT
CLNSRC OMIM Allelic Variant
CLNACC RCV000043553.5,