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rs397508452

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508452(C;C)
Make rs397508452(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117603784
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508452
ebirs397508452
HLIrs397508452
Exacrs397508452
Varsomers397508452
Maprs397508452
PheGenIrs397508452
hapmaprs397508452
1000 genomesrs397508452
hgdprs397508452
ensemblrs397508452
gopubmedrs397508452
geneviewrs397508452
scholarrs397508452
googlers397508452
pharmgkbrs397508452
gwascentralrs397508452
openSNPrs397508452
23andMers397508452
23andMe allrs397508452
SNP Nexus

SNPshotrs397508452
SNPdbers397508452
MSV3drs397508452
GWAS Ctlgrs397508452
Max Magnitude0
ClinVar
Risk rs397508452(C;C)
Alt rs397508452(C;C)
Reference rs397508452(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117243838T>C
CLNSRC ClinVar
CLNACC RCV000046711.2,