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rs137852710

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852710(A;A)
Make rs137852710(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position23380493
GeneSCNN1B
is asnp
is mentioned by
dbSNPrs137852710
ebirs137852710
HLIrs137852710
Exacrs137852710
Varsomers137852710
Maprs137852710
PheGenIrs137852710
hapmaprs137852710
1000 genomesrs137852710
hgdprs137852710
ensemblrs137852710
gopubmedrs137852710
geneviewrs137852710
scholarrs137852710
googlers137852710
pharmgkbrs137852710
gwascentralrs137852710
openSNPrs137852710
23andMers137852710
23andMe allrs137852710
SNP Nexus

SNPshotrs137852710
SNPdbers137852710
MSV3drs137852710
GWAS Ctlgrs137852710
Max Magnitude0
OMIM600760
Desc
Variant0012
Relatedalso
ClinVar
Risk rs137852710(A;A)
Alt rs137852710(A;A)
Reference rs137852710(G;G)
Significance Pathogenic
Disease Bronchiectasis
Variation info
Gene SCNN1B
CLNDBN Bronchiectasis
Reversed 0
HGVS NC_000016.9:g.23391814G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009389.3,