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rs587777658

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777658(-;-)
Make rs587777658(-;T)
ReferenceGRCh38 38.1/142
Chromosome22
Position20425445
GeneSCARF2
is asnp
is mentioned by
dbSNPrs587777658
ebirs587777658
HLIrs587777658
Exacrs587777658
Varsomers587777658
Maprs587777658
PheGenIrs587777658
hapmaprs587777658
1000 genomesrs587777658
hgdprs587777658
ensemblrs587777658
gopubmedrs587777658
geneviewrs587777658
scholarrs587777658
googlers587777658
pharmgkbrs587777658
gwascentralrs587777658
openSNPrs587777658
23andMers587777658
23andMe allrs587777658
SNP Nexus

SNPshotrs587777658
SNPdbers587777658
MSV3drs587777658
GWAS Ctlgrs587777658
Max Magnitude0
ClinVar
Risk rs587777658(TG,G;TG,G)
Alt rs587777658(TG,G;TG,G)
Reference rs587777658(AG;AG)
Significance Pathogenic
Disease Marden Walker like syndrome
Variation info
Gene SCARF2
CLNDBN Marden Walker like syndrome
Reversed 1
HGVS NC_000022.10:g.20779735delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000133556.3,