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rs1057517826

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517826(G;G)
Make rs1057517826(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position6394273
GeneSMPD1
is asnp
is mentioned by
dbSNPrs1057517826
dbSNP (old)rs1057517826
ClinGenrs1057517826
ebirs1057517826
HLIrs1057517826
Exacrs1057517826
Gnomadrs1057517826
Varsomers1057517826
Maprs1057517826
PheGenIrs1057517826
Biobankrs1057517826
1000 genomesrs1057517826
hgdprs1057517826
ensemblrs1057517826
gopubmedrs1057517826
geneviewrs1057517826
scholarrs1057517826
googlers1057517826
pharmgkbrs1057517826
gwascentralrs1057517826
openSNPrs1057517826
23andMers1057517826
23andMe allrs1057517826
SNPshotrs1057517826
SNPdbers1057517826
MSV3drs1057517826
GWAS Ctlgrs1057517826
Max Magnitude0
ClinVar
Risk rs1057517826(G;G)
Alt rs1057517826(G;G)
Reference Rs1057517826(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SMPD1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.6415503T>G
CLNSRC
CLNACC RCV000414036.1,