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rs17095355

From SNPedia

Orientationplus
Stabilizedplus
Make rs17095355(C;C)
Make rs17095355(C;T)
Make rs17095355(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position109975992
GeneLOC100505933
is asnp
is mentioned by
dbSNPrs17095355
ebirs17095355
HLIrs17095355
Exacrs17095355
Varsomers17095355
Maprs17095355
PheGenIrs17095355
hapmaprs17095355
1000 genomesrs17095355
hgdprs17095355
ensemblrs17095355
gopubmedrs17095355
geneviewrs17095355
scholarrs17095355
googlers17095355
pharmgkbrs17095355
gwascentralrs17095355
openSNPrs17095355
23andMers17095355
23andMe allrs17095355
SNP Nexus

SNPshotrs17095355
SNPdbers17095355
MSV3drs17095355
GWAS Ctlgrs17095355
GMAF0.2553
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20460270OA-icon.png]
Trait Biliary atresia
Title Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2
Risk Allele T
P-val 7E-9
Odds Ratio 1.77 [1.38-2.26]


[PMID 22118303] Association of X-prolyl aminopeptidase 1 rs17095355 polymorphism with biliary atresia in Thai children


[PMID 23872602] Common genetic variants regulating ADD3 gene expression alter biliary atresia risk


[PMID 25285724OA-icon.png] Association between single nucleotide polymorphisms in the ADD3 gene and susceptibility to biliary atresia