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rs587776862

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GCCTGAGGAGGA;GCCTGAGGAGGA) 0 common in clinvar
Make rs587776862(GCCTGAGGAGGA;T)
Make rs587776862(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position239908624
GeneCHRM3
is asnp
is mentioned by
dbSNPrs587776862
ebirs587776862
HLIrs587776862
Exacrs587776862
Varsomers587776862
Maprs587776862
PheGenIrs587776862
hapmaprs587776862
1000 genomesrs587776862
hgdprs587776862
ensemblrs587776862
gopubmedrs587776862
geneviewrs587776862
scholarrs587776862
googlers587776862
pharmgkbrs587776862
gwascentralrs587776862
openSNPrs587776862
23andMers587776862
23andMe allrs587776862
SNP Nexus

SNPshotrs587776862
SNPdbers587776862
MSV3drs587776862
GWAS Ctlgrs587776862
Max Magnitude0
ClinVar
Risk rs587776862(T;T)
Alt rs587776862(T;T)
Reference rs587776862(GCCTGAGGAGGA;GCCTGAGGAGGA)
Significance Pathogenic
Disease Prune belly syndrome
Variation info
Gene CHRM3
CLNDBN Prune belly syndrome
Reversed 0
HGVS NC_000001.10:g.240071924_240071935delGCCTGAGGAGGAinsT
CLNSRC OMIM Allelic Variant
CLNACC RCV000022466.29,