Have questions? Visit https://www.reddit.com/r/SNPedia

rs2236405

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs2236405(A;A)
Make rs2236405(A;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position95449290
GenePTCH1
is asnp
is mentioned by
dbSNPrs2236405
ebirs2236405
HLIrs2236405
Exacrs2236405
Varsomers2236405
Maprs2236405
PheGenIrs2236405
hapmaprs2236405
1000 genomesrs2236405
hgdprs2236405
ensemblrs2236405
gopubmedrs2236405
geneviewrs2236405
scholarrs2236405
googlers2236405
pharmgkbrs2236405
gwascentralrs2236405
openSNPrs2236405
23andMers2236405
23andMe allrs2236405
SNP Nexus

SNPshotrs2236405
SNPdbers2236405
MSV3drs2236405
GWAS Ctlgrs2236405
GMAF0.07943
Max Magnitude0
? (A;A) (A;T) (T;T) 28
[PMID 24073265OA-icon.png] Common Genetic Variations in Patched1 (PTCH1) Gene and Risk of Hirschsprung Disease in the Han Chinese Population


ClinVar
Risk rs2236405(A;A)
Alt rs2236405(A;A)
Reference rs2236405(T;T)
Significance Non-pathogenic
Disease not specified not provided
Variation info
Gene PTCH1
CLNDBN not specified not provided
Reversed 0
HGVS NC_000009.11:g.98211572T>A
CLNSRC ClinVar GeneDx
CLNACC RCV000121893.2, RCV000127647.1,