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rs1057518353

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518353(A;G)
Make rs1057518353(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position151666403
GeneNEB
is asnp
is mentioned by
dbSNPrs1057518353
dbSNP (old)rs1057518353
ClinGenrs1057518353
ebirs1057518353
HLIrs1057518353
Exacrs1057518353
Gnomadrs1057518353
Varsomers1057518353
LitVarrs1057518353
Maprs1057518353
PheGenIrs1057518353
Biobankrs1057518353
1000 genomesrs1057518353
hgdprs1057518353
ensemblrs1057518353
gopubmedrs1057518353
geneviewrs1057518353
scholarrs1057518353
googlers1057518353
pharmgkbrs1057518353
gwascentralrs1057518353
openSNPrs1057518353
23andMers1057518353
23andMe allrs1057518353
SNPshotrs1057518353
SNPdbers1057518353
MSV3drs1057518353
GWAS Ctlgrs1057518353
Max Magnitude0
ClinVar
Risk rs1057518353(G;G)
Alt rs1057518353(G;G)
Reference Rs1057518353(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NEB
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.152522917T>C
CLNSRC
CLNACC RCV000413634.1,