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rs72654338

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72654338(A;A)
Make rs72654338(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position23367959
GeneSCNN1B
is asnp
is mentioned by
dbSNPrs72654338
ebirs72654338
HLIrs72654338
Exacrs72654338
Varsomers72654338
Maprs72654338
PheGenIrs72654338
hapmaprs72654338
1000 genomesrs72654338
hgdprs72654338
ensemblrs72654338
gopubmedrs72654338
geneviewrs72654338
scholarrs72654338
googlers72654338
pharmgkbrs72654338
gwascentralrs72654338
openSNPrs72654338
23andMers72654338
23andMe allrs72654338
SNP Nexus

SNPshotrs72654338
SNPdbers72654338
MSV3drs72654338
GWAS Ctlgrs72654338
Max Magnitude0
OMIM600760
Desc
Variant0011
Relatedalso


ClinVar
Risk rs72654338(A;A)
Alt rs72654338(A;A)
Reference rs72654338(G;G)
Significance Pathogenic
Disease Bronchiectasis
Variation info
Gene SCNN1B
CLNDBN Bronchiectasis
Reversed 0
HGVS NC_000016.9:g.23379280G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009388.2,