Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057517977

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517977(C;T)
Make rs1057517977(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position151636283
GeneNEB
is asnp
is mentioned by
dbSNPrs1057517977
dbSNP (old)rs1057517977
ClinGenrs1057517977
ebirs1057517977
HLIrs1057517977
Exacrs1057517977
Gnomadrs1057517977
Varsomers1057517977
Maprs1057517977
PheGenIrs1057517977
Biobankrs1057517977
1000 genomesrs1057517977
hgdprs1057517977
ensemblrs1057517977
gopubmedrs1057517977
geneviewrs1057517977
scholarrs1057517977
googlers1057517977
pharmgkbrs1057517977
gwascentralrs1057517977
openSNPrs1057517977
23andMers1057517977
23andMe allrs1057517977
SNPshotrs1057517977
SNPdbers1057517977
MSV3drs1057517977
GWAS Ctlgrs1057517977
Max Magnitude0
ClinVar
Risk rs1057517977(T;T)
Alt rs1057517977(T;T)
Reference Rs1057517977(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene NEB
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.152492797G>A
CLNSRC
CLNACC RCV000413859.1,