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rs587777315

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777315(C;G)
Make rs587777315(G;G)
ReferenceGRCh38 38.1/142
Chromosome15
Position64974732
GeneSPG21
is asnp
is mentioned by
dbSNPrs587777315
ebirs587777315
HLIrs587777315
Exacrs587777315
Varsomers587777315
Maprs587777315
PheGenIrs587777315
hapmaprs587777315
1000 genomesrs587777315
hgdprs587777315
ensemblrs587777315
gopubmedrs587777315
geneviewrs587777315
scholarrs587777315
googlers587777315
pharmgkbrs587777315
gwascentralrs587777315
openSNPrs587777315
23andMers587777315
23andMe allrs587777315
SNP Nexus

SNPshotrs587777315
SNPdbers587777315
MSV3drs587777315
GWAS Ctlgrs587777315
Max Magnitude0
ClinVar
Risk rs587777315(G,T;G,T)
Alt rs587777315(G,T;G,T)
Reference rs587777315(C;C)
Significance Pathogenic
Disease Mast syndrome
Variation info
Gene SPG21
CLNDBN Mast syndrome
Reversed 0
HGVS NC_000015.9:g.65267070C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000114945.2,