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rs1057518200

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518200(A;A)
Make rs1057518200(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position151570249
GeneNEB
is asnp
is mentioned by
dbSNPrs1057518200
dbSNP (old)rs1057518200
ClinGenrs1057518200
ebirs1057518200
HLIrs1057518200
Exacrs1057518200
Gnomadrs1057518200
Varsomers1057518200
Maprs1057518200
PheGenIrs1057518200
Biobankrs1057518200
1000 genomesrs1057518200
hgdprs1057518200
ensemblrs1057518200
gopubmedrs1057518200
geneviewrs1057518200
scholarrs1057518200
googlers1057518200
pharmgkbrs1057518200
gwascentralrs1057518200
openSNPrs1057518200
23andMers1057518200
23andMe allrs1057518200
SNPshotrs1057518200
SNPdbers1057518200
MSV3drs1057518200
GWAS Ctlgrs1057518200
Max Magnitude0
ClinVar
Risk rs1057518200(A;A)
Alt rs1057518200(A;A)
Reference Rs1057518200(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NEB
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.152426763C>T
CLNSRC
CLNACC RCV000413503.1,