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

rs587777322

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777322(-;-)
Make rs587777322(-;A)
ReferenceGRCh38 38.1/142
Chromosome4
Position155713181
GeneGUCY1A3
is asnp
is mentioned by
dbSNPrs587777322
dbSNP (classic)rs587777322
ClinGenrs587777322
ebirs587777322
HLIrs587777322
Exacrs587777322
Gnomadrs587777322
Varsomers587777322
LitVarrs587777322
Maprs587777322
PheGenIrs587777322
Biobankrs587777322
1000 genomesrs587777322
hgdprs587777322
ensemblrs587777322
geneviewrs587777322
scholarrs587777322
googlers587777322
pharmgkbrs587777322
gwascentralrs587777322
openSNPrs587777322
23andMers587777322
SNPshotrs587777322
SNPdbers587777322
MSV3drs587777322
GWAS Ctlgrs587777322
Max Magnitude0
ClinVar
Risk rs587777322(-;-)
Alt rs587777322(-;-)
Reference Rs587777322(A;A)
Significance Pathogenic
Disease Moyamoya disease 6 with achalasia
Variation info
Gene GUCY1A3
CLNDBN Moyamoya disease 6 with achalasia
Reversed 0
HGVS NC_000004.11:g.156634333delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000114954.2,