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rs137853581

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853581(C;T)
Make rs137853581(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position169703414
GeneSELL
is asnp
is mentioned by
dbSNPrs137853581
ebirs137853581
HLIrs137853581
Exacrs137853581
Varsomers137853581
Maprs137853581
PheGenIrs137853581
hapmaprs137853581
1000 genomesrs137853581
hgdprs137853581
ensemblrs137853581
gopubmedrs137853581
geneviewrs137853581
scholarrs137853581
googlers137853581
pharmgkbrs137853581
gwascentralrs137853581
openSNPrs137853581
23andMers137853581
23andMe allrs137853581
SNP Nexus

SNPshotrs137853581
SNPdbers137853581
MSV3drs137853581
GWAS Ctlgrs137853581
Max Magnitude0
OMIM153240
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137853581(T;T)
Alt rs137853581(T;T)
Reference rs137853581(C;C)
Significance Untested
Disease
Variation info
Gene SELL
CLNDBN
Reversed 1
HGVS NC_000001.10:g.169672555G>A
CLNSRC OMIM Allelic Variant
CLNACC