Have questions? Visit https://www.reddit.com/r/SNPedia

rs137852705

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852705(C;T)
Make rs137852705(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position23380731
GeneSCNN1B
is asnp
is mentioned by
dbSNPrs137852705
ebirs137852705
HLIrs137852705
Exacrs137852705
Varsomers137852705
Maprs137852705
PheGenIrs137852705
hapmaprs137852705
1000 genomesrs137852705
hgdprs137852705
ensemblrs137852705
gopubmedrs137852705
geneviewrs137852705
scholarrs137852705
googlers137852705
pharmgkbrs137852705
gwascentralrs137852705
openSNPrs137852705
23andMers137852705
23andMe allrs137852705
SNP Nexus

SNPshotrs137852705
SNPdbers137852705
MSV3drs137852705
GWAS Ctlgrs137852705
Max Magnitude0
OMIM600760
Desc
Variant0002
Relatedalso
OMIM600760
Desc
Variant0008
Relatedalso
ClinVar
Risk rs137852705(G,T;G,T)
Alt rs137852705(G,T;G,T)
Reference rs137852705(C;C)
Significance Untested
Disease
Variation info
Gene SCNN1B
CLNDBN
Reversed 0
HGVS NC_000016.9:g.23392052C>G; NC_000016.9:g.23392052C>T
CLNSRC
CLNACC