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rs779204655

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs779204655(C;T)
Make rs779204655(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position72891406
GeneSPR
is asnp
is mentioned by
dbSNPrs779204655
ebirs779204655
HLIrs779204655
Exacrs779204655
Varsomers779204655
Maprs779204655
PheGenIrs779204655
hapmaprs779204655
1000 genomesrs779204655
hgdprs779204655
ensemblrs779204655
gopubmedrs779204655
geneviewrs779204655
scholarrs779204655
googlers779204655
pharmgkbrs779204655
gwascentralrs779204655
openSNPrs779204655
23andMers779204655
23andMe allrs779204655
SNP Nexus

SNPshotrs779204655
SNPdbers779204655
MSV3drs779204655
GWAS Ctlgrs779204655
Max Magnitude0
ClinVar
Risk rs779204655(T;T)
Alt rs779204655(T;T)
Reference rs779204655(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SPR
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.73118535C>T
CLNSRC
CLNACC RCV000224347.1,