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rs397508354

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397508354(G;T)
Make rs397508354(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592400
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508354
ebirs397508354
HLIrs397508354
Exacrs397508354
Varsomers397508354
Maprs397508354
PheGenIrs397508354
hapmaprs397508354
1000 genomesrs397508354
hgdprs397508354
ensemblrs397508354
gopubmedrs397508354
geneviewrs397508354
scholarrs397508354
googlers397508354
pharmgkbrs397508354
gwascentralrs397508354
openSNPrs397508354
23andMers397508354
23andMe allrs397508354
SNP Nexus

SNPshotrs397508354
SNPdbers397508354
MSV3drs397508354
GWAS Ctlgrs397508354
Max Magnitude0
ClinVar
Risk rs397508354(T;T)
Alt rs397508354(T;T)
Reference rs397508354(G;G)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232454G>T
CLNSRC ClinVar
CLNACC RCV000046557.2,