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rs587776902

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
(TGA;TGA) 0 common in clinvar
Make rs587776902(-;-)
Make rs587776902(-;CA)
ReferenceGRCh38 38.1/142
Chromosome22
Position20429631
GeneSCARF2
is asnp
is mentioned by
dbSNPrs587776902
ebirs587776902
HLIrs587776902
Exacrs587776902
Varsomers587776902
Maprs587776902
PheGenIrs587776902
hapmaprs587776902
1000 genomesrs587776902
hgdprs587776902
ensemblrs587776902
gopubmedrs587776902
geneviewrs587776902
scholarrs587776902
googlers587776902
pharmgkbrs587776902
gwascentralrs587776902
openSNPrs587776902
23andMers587776902
23andMe allrs587776902
SNP Nexus

SNPshotrs587776902
SNPdbers587776902
MSV3drs587776902
GWAS Ctlgrs587776902
Max Magnitude0
ClinVar
Risk rs587776902(CAA,A;CAA,A)
Alt rs587776902(CAA,A;CAA,A)
Reference rs587776902(TGA;TGA)
Significance Pathogenic
Disease Marden Walker like syndrome
Variation info
Gene SCARF2
CLNDBN Marden Walker like syndrome
Reversed 1
HGVS NC_000022.10:g.20783918_20783919delCA
CLNSRC OMIM Allelic Variant
CLNACC RCV000024041.5,