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rs397508407

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508407(A;A)
Make rs397508407(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117595060
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508407
ebirs397508407
HLIrs397508407
Exacrs397508407
Varsomers397508407
Maprs397508407
PheGenIrs397508407
hapmaprs397508407
1000 genomesrs397508407
hgdprs397508407
ensemblrs397508407
gopubmedrs397508407
geneviewrs397508407
scholarrs397508407
googlers397508407
pharmgkbrs397508407
gwascentralrs397508407
openSNPrs397508407
23andMers397508407
23andMe allrs397508407
SNP Nexus

SNPshotrs397508407
SNPdbers397508407
MSV3drs397508407
GWAS Ctlgrs397508407
Max Magnitude0
ClinVar
Risk rs397508407(A;A)
Alt rs397508407(A;A)
Reference rs397508407(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117235114T>A
CLNSRC ClinVar
CLNACC RCV000046633.2,