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rs587776871

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776871(A;A)
Make rs587776871(A;C)
ReferenceGRCh38 38.1/142
Chromosome12
Position14622087
GeneC12orf60, GUCY2C
is asnp
is mentioned by
dbSNPrs587776871
dbSNP (classic)rs587776871
ClinGenrs587776871
ebirs587776871
HLIrs587776871
Exacrs587776871
Gnomadrs587776871
Varsomers587776871
LitVarrs587776871
Maprs587776871
PheGenIrs587776871
Biobankrs587776871
1000 genomesrs587776871
hgdprs587776871
ensemblrs587776871
geneviewrs587776871
scholarrs587776871
googlers587776871
pharmgkbrs587776871
gwascentralrs587776871
openSNPrs587776871
23andMers587776871
SNPshotrs587776871
SNPdbers587776871
MSV3drs587776871
GWAS Ctlgrs587776871
Max Magnitude0
ClinVar
Risk rs587776871(A;A)
Alt rs587776871(A;A)
Reference Rs587776871(C;C)
Significance Pathogenic
Disease Diarrhea 6
Variation info
Gene GUCY2C
CLNDBN Diarrhea 6
Reversed 0
HGVS NC_000012.11:g.14775021C>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000023094.2,