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rs397508689

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508689(C;T)
Make rs397508689(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117665490
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508689
ClinGenrs397508689
ebirs397508689
HLIrs397508689
Exacrs397508689
Varsomers397508689
Maprs397508689
PheGenIrs397508689
hapmaprs397508689
1000 genomesrs397508689
hgdprs397508689
ensemblrs397508689
gopubmedrs397508689
geneviewrs397508689
scholarrs397508689
googlers397508689
pharmgkbrs397508689
gwascentralrs397508689
openSNPrs397508689
23andMers397508689
23andMe allrs397508689
SNP Nexus

SNPshotrs397508689
SNPdbers397508689
MSV3drs397508689
GWAS Ctlgrs397508689
Max Magnitude0
ClinVar
Risk rs397508689(T;T)
Alt rs397508689(T;T)
Reference Rs397508689(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117305544C>T
CLNSRC ClinVar
CLNACC RCV000047093.2,