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rs1057521084

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057521084(C;C)
Make rs1057521084(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position184137679
GeneEIF2B5
is asnp
is mentioned by
dbSNPrs1057521084
dbSNP (old)rs1057521084
ClinGenrs1057521084
ebirs1057521084
HLIrs1057521084
Exacrs1057521084
Gnomadrs1057521084
Varsomers1057521084
Maprs1057521084
PheGenIrs1057521084
Biobankrs1057521084
1000 genomesrs1057521084
hgdprs1057521084
ensemblrs1057521084
gopubmedrs1057521084
geneviewrs1057521084
scholarrs1057521084
googlers1057521084
pharmgkbrs1057521084
gwascentralrs1057521084
openSNPrs1057521084
23andMers1057521084
23andMe allrs1057521084
SNPshotrs1057521084
SNPdbers1057521084
MSV3drs1057521084
GWAS Ctlgrs1057521084
Max Magnitude0
ClinVar
Risk rs1057521084(C;C)
Alt rs1057521084(C;C)
Reference Rs1057521084(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EIF2B5
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.183855467T>C
CLNSRC
CLNACC RCV000439475.1,