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rs397508517

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508517(C;T)
Make rs397508517(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117611652
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508517
ebirs397508517
HLIrs397508517
Exacrs397508517
Varsomers397508517
Maprs397508517
PheGenIrs397508517
hapmaprs397508517
1000 genomesrs397508517
hgdprs397508517
ensemblrs397508517
gopubmedrs397508517
geneviewrs397508517
scholarrs397508517
googlers397508517
pharmgkbrs397508517
gwascentralrs397508517
openSNPrs397508517
23andMers397508517
23andMe allrs397508517
SNP Nexus

SNPshotrs397508517
SNPdbers397508517
MSV3drs397508517
GWAS Ctlgrs397508517
Max Magnitude0
ClinVar
Risk rs397508517(T;T)
Alt rs397508517(T;T)
Reference rs397508517(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117251706C>T
CLNSRC ClinVar
CLNACC RCV000046827.2,