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

rs587784572

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784572(A;A)
Make rs587784572(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position14641142
GeneGUCY2C
is asnp
is mentioned by
dbSNPrs587784572
ebirs587784572
HLIrs587784572
Exacrs587784572
Varsomers587784572
Maprs587784572
PheGenIrs587784572
hapmaprs587784572
1000 genomesrs587784572
hgdprs587784572
ensemblrs587784572
gopubmedrs587784572
geneviewrs587784572
scholarrs587784572
googlers587784572
pharmgkbrs587784572
gwascentralrs587784572
openSNPrs587784572
23andMers587784572
23andMe allrs587784572
SNP Nexus

SNPshotrs587784572
SNPdbers587784572
MSV3drs587784572
GWAS Ctlgrs587784572
Max Magnitude0
ClinVar
Risk rs587784572(A;A)
Alt rs587784572(A;A)
Reference rs587784572(G;G)
Significance Pathogenic
Disease Meconium ileus
Variation info
Gene GUCY2C
CLNDBN Meconium ileus
Reversed 1
HGVS NC_000012.11:g.14794076C>T
CLNSRC GUCY2C database
CLNACC RCV000148339.1,