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rs397508462

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508462(A;C)
Make rs397508462(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117606701
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508462
ebirs397508462
HLIrs397508462
Exacrs397508462
Varsomers397508462
Maprs397508462
PheGenIrs397508462
hapmaprs397508462
1000 genomesrs397508462
hgdprs397508462
ensemblrs397508462
gopubmedrs397508462
geneviewrs397508462
scholarrs397508462
googlers397508462
pharmgkbrs397508462
gwascentralrs397508462
openSNPrs397508462
23andMers397508462
23andMe allrs397508462
SNP Nexus

SNPshotrs397508462
SNPdbers397508462
MSV3drs397508462
GWAS Ctlgrs397508462
Max Magnitude0
ClinVar
Risk rs397508462(C,T;C,T)
Alt rs397508462(C,T;C,T)
Reference rs397508462(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117246755A>C; NC_000007.13:g.117246755A>T
CLNSRC ClinVar
CLNACC RCV000046727.2, RCV000046728.2,