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rs1057524581

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524581(G;T)
Make rs1057524581(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position151688291
GeneNEB
is asnp
is mentioned by
dbSNPrs1057524581
dbSNP (old)rs1057524581
ClinGenrs1057524581
ebirs1057524581
HLIrs1057524581
Exacrs1057524581
Gnomadrs1057524581
Varsomers1057524581
Maprs1057524581
PheGenIrs1057524581
Biobankrs1057524581
1000 genomesrs1057524581
hgdprs1057524581
ensemblrs1057524581
gopubmedrs1057524581
geneviewrs1057524581
scholarrs1057524581
googlers1057524581
pharmgkbrs1057524581
gwascentralrs1057524581
openSNPrs1057524581
23andMers1057524581
23andMe allrs1057524581
SNPshotrs1057524581
SNPdbers1057524581
MSV3drs1057524581
GWAS Ctlgrs1057524581
Max Magnitude0
ClinVar
Risk rs1057524581(A;A) rs1057524581(T;T)
Alt rs1057524581(A;A) rs1057524581(T;T)
Reference Rs1057524581(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NEB
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.152544805C>A; NC_000002.11:g.152544805C>T
CLNSRC
CLNACC RCV000437465.1, RCV000487268.1,