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rs397508404

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508404(A;A)
Make rs397508404(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117595039
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508404
ebirs397508404
HLIrs397508404
Exacrs397508404
Varsomers397508404
Maprs397508404
PheGenIrs397508404
hapmaprs397508404
1000 genomesrs397508404
hgdprs397508404
ensemblrs397508404
gopubmedrs397508404
geneviewrs397508404
scholarrs397508404
googlers397508404
pharmgkbrs397508404
gwascentralrs397508404
openSNPrs397508404
23andMers397508404
23andMe allrs397508404
SNP Nexus

SNPshotrs397508404
SNPdbers397508404
MSV3drs397508404
GWAS Ctlgrs397508404
Max Magnitude0
ClinVar
Risk rs397508404(A;A)
Alt rs397508404(A;A)
Reference rs397508404(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117235093T>A
CLNSRC ClinVar
CLNACC RCV000046630.2,