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rs201553266

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201553266(C;T)
Make rs201553266(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position151551738
GeneNEB
is asnp
is mentioned by
dbSNPrs201553266
ebirs201553266
HLIrs201553266
Exacrs201553266
Varsomers201553266
Maprs201553266
PheGenIrs201553266
hapmaprs201553266
1000 genomesrs201553266
hgdprs201553266
ensemblrs201553266
gopubmedrs201553266
geneviewrs201553266
scholarrs201553266
googlers201553266
pharmgkbrs201553266
gwascentralrs201553266
openSNPrs201553266
23andMers201553266
23andMe allrs201553266
SNP Nexus

SNPshotrs201553266
SNPdbers201553266
MSV3drs201553266
GWAS Ctlgrs201553266
Max Magnitude0
ClinVar
Risk rs201553266(T;T)
Alt rs201553266(T;T)
Reference rs201553266(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene NEB
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.152408252C>T
CLNSRC
CLNACC RCV000224886.1,