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rs587777657

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777657(A;G)
Make rs587777657(G;G)
ReferenceGRCh38 38.1/142
Chromosome22
Position20431972
GeneSCARF2
is asnp
is mentioned by
dbSNPrs587777657
ebirs587777657
HLIrs587777657
Exacrs587777657
Varsomers587777657
Maprs587777657
PheGenIrs587777657
hapmaprs587777657
1000 genomesrs587777657
hgdprs587777657
ensemblrs587777657
gopubmedrs587777657
geneviewrs587777657
scholarrs587777657
googlers587777657
pharmgkbrs587777657
gwascentralrs587777657
openSNPrs587777657
23andMers587777657
23andMe allrs587777657
SNP Nexus

SNPshotrs587777657
SNPdbers587777657
MSV3drs587777657
GWAS Ctlgrs587777657
Max Magnitude0
ClinVar
Risk rs587777657(A,G;A,G)
Alt rs587777657(A,G;A,G)
Reference rs587777657(T;T)
Significance Pathogenic
Disease Marden Walker like syndrome
Variation info
Gene SCARF2
CLNDBN Marden Walker like syndrome
Reversed 1
HGVS NC_000022.10:g.20786259A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000133555.3,