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rs397508467

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508467(C;T)
Make rs397508467(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117530921
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508467
ebirs397508467
HLIrs397508467
Exacrs397508467
Varsomers397508467
Maprs397508467
PheGenIrs397508467
hapmaprs397508467
1000 genomesrs397508467
hgdprs397508467
ensemblrs397508467
gopubmedrs397508467
geneviewrs397508467
scholarrs397508467
googlers397508467
pharmgkbrs397508467
gwascentralrs397508467
openSNPrs397508467
23andMers397508467
23andMe allrs397508467
SNP Nexus

SNPshotrs397508467
SNPdbers397508467
MSV3drs397508467
GWAS Ctlgrs397508467
Max Magnitude0
ClinVar
Risk rs397508467(T;T)
Alt rs397508467(T;T)
Reference rs397508467(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117170975C>T
CLNSRC ClinVar
CLNACC RCV000046735.2,