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rs587777550

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587777550(-;-)
Make rs587777550(-;G)
Make rs587777550(G;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position47029255
GeneTTC7A
is asnp
is mentioned by
dbSNPrs587777550
ebirs587777550
HLIrs587777550
Exacrs587777550
Varsomers587777550
Maprs587777550
PheGenIrs587777550
hapmaprs587777550
1000 genomesrs587777550
hgdprs587777550
ensemblrs587777550
gopubmedrs587777550
geneviewrs587777550
scholarrs587777550
googlers587777550
pharmgkbrs587777550
gwascentralrs587777550
openSNPrs587777550
23andMers587777550
23andMe allrs587777550
SNP Nexus

SNPshotrs587777550
SNPdbers587777550
MSV3drs587777550
GWAS Ctlgrs587777550
Max Magnitude0
ClinVar
Risk rs587777550(G;G)
Alt rs587777550(G;G)
Reference rs587777550(;)
Significance Pathogenic
Disease Multiple gastrointestinal atresias
Variation info
Gene TTC7A
CLNDBN Multiple gastrointestinal atresias
Reversed 0
HGVS NC_000002.11:g.47256394_47256395insG
CLNSRC OMIM Allelic Variant
CLNACC RCV000128797.3,