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rs35731153

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs35731153(C;G)
Make rs35731153(G;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position23348844
GeneSCNN1B
is asnp
is mentioned by
dbSNPrs35731153
ebirs35731153
HLIrs35731153
Exacrs35731153
Varsomers35731153
Maprs35731153
PheGenIrs35731153
hapmaprs35731153
1000 genomesrs35731153
hgdprs35731153
ensemblrs35731153
gopubmedrs35731153
geneviewrs35731153
scholarrs35731153
googlers35731153
pharmgkbrs35731153
gwascentralrs35731153
openSNPrs35731153
23andMers35731153
23andMe allrs35731153
SNP Nexus

SNPshotrs35731153
SNPdbers35731153
MSV3drs35731153
GWAS Ctlgrs35731153
GMAF0.0004591
Max Magnitude0
OMIM600760
Desc
Variant0015
Relatedalso
ClinVar
Risk rs35731153(G;G)
Alt rs35731153(G;G)
Reference rs35731153(C;C)
Significance Pathogenic
Disease Bronchiectasis not specified
Variation info
Gene SCNN1B
CLNDBN Bronchiectasis not specified
Reversed 0
HGVS NC_000016.9:g.23360165C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000009392.2, RCV000175586.1,